EFFECTS OF SELECTED HERBICIDES ON BACTERIAL POPULATIONS IN NONTREATED AND TREATED WATER1

ABSTRACT: Bacterial populations in nontreated and herbicide-treated waters were subjected to three different herbicides. Diuron, dichlobenil, and diquat were added (100 mg/l) to water samples from two fresh water lakes and two herbicide-treated ponds. Total numbers of bacteria were monitored. Bacterial populations in fresh lake water decreased after herbicide additions; however, final populations were significantly greater than the controls. Similar observations were recorded for bacteria in dichlobenil- and diuron-treated waters. Selective enrichment is probably expressed in these experiments.     

HERBICIDES AND TRANSFORMATION PRODUCTS IN SURFACE WATERS OF THE MIDWESTERN UNITED STATES1

ABSTRACT: Most herbicides applied to crops are adsorbed by plants or transformed (degraded) in the soil, but small fractions are lost from fields and either move to streams in overland runoff, near surface flow, or subsurface drains, or they infiltrate slowly to ground water. Herbicide transformation products (TPs) can be more or less mobile and more or less toxic in the environment than their source herbicides. To obtain information on the concentrations of selected herbicides and TPs in surface waters of the Midwestern United States, 151 water samples were collected from 71 streams and five reservoir outflows in 1998. These samples were analyzed for 13 herbicides and 10 herbicide TPs. Herbicide TPs were found to occur as frequently or more frequently than source herbicides and at concentrations that were often larger than their source herbicides. Most samples contained a mixture of more than 10 different herbicides or TPs. The ratios of TPs to herbicide concentrations can be used to determine the source of herbicides in streams. Results of a two‐component mixing model suggest that on average 90 percent or more of the herbicide mass in Midwestern streams during early summer runoff events originates from the runoff and 10 percent or less comes from increased ground water discharge.     

Fate of diuron and linuron in a field lysimeter experiment

The environmental fate of herbicides can be studied at different levels: in the lab with disturbed or undisturbed soil columns or in the field with suction cup lysimeters or soil enclosure lysimeters. A field lysimeter experiment with 10 soil enclosures was performed to evaluate the mass balance in different environmental compartments of the phenylurea herbicides diuron [3-(3,4-diclorophenyl)-1,1-dimethyl-urea] and linuron [3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea]. After application on the agricultural soil, the herbicides were searched for in soil, pore water, and air samples. Soil and water samples were collected at different depths of the soil profile and analyzed to determine residual concentrations of both the parent compounds and of their main transformation products, to verify their persistence and their leaching capacity. Air volatilization was calculated using the theoretical profile shape method. The herbicides were detected only in the surface layer (0-10 cm) of soil. In this layer, diuron was reduced to 50% of its initial concentration at the end of the experiment, while linuron was still 70% present after 245 d. The main metabolites detected were DCPMU [3-(3,4-dichlorophenyl)-1-methylurea] and DCA (3,4-dichloroaniline). In soil pore water, diuron and linuron were detected at depths of 20 and 40 cm, although in very low concentrations. Therefore the leaching of these herbicides was quite low in this experiment. Moreover, volatilization losses were inconsequential. The calculated total mass balance showed a high persistence of linuron and diuron in the soil, a low mobility in soil pore water (less than 0.5% in leachate water), and a negligible volatilization effect. The application of the Pesticide Leaching Model (PELMO) showed similar low mobility of the chemicals in soil and water, but overestimated their volatilization and their degradation to the metabolite DCPMU. In conclusion, the use of soil enclosure lysimeters proved to be a good experimental design for studying mobility and transport processes of herbicides in field conditions.     

Contribution of hydrolysis in the abiotic attenuation of RDX and HMX in coastal waters

Sinking of military ships, dumping of munitions during the two World Wars, and military training have resulted in the undersea deposition of numerous unexploded ordnances (UXOs). Leaching of energetic compounds such as hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) from these UXOs may cause adverse ecological effects so that the long-term fate of these chemicals in the sea should be known. The present study assesses the contribution of alkaline hydrolysis into the natural attenuation of RDX and HMX in coastal waters. Alkaline hydrolysis rates were shown to be unaffected by the presence of sodium chloride, the most common component in marine waters. Kinetic parameters (E(a), ln A, k(2)) quantified for the alkaline hydrolysis of RDX and HMX in deionized water (30-50 degrees C, pH 10-12) agreed relatively well with abiotic degradation rates determined in sterilized natural coastal waters (50 and 60 degrees C, variable salinity) even if the latter were generally slightly faster than the former. Furthermore, similar products (HCHO, NO(2)(-), O(2)NNHCH(2)NHCHO) were obtained on alkaline hydrolysis in deionized water and abiotic degradation in coastal waters. These two findings suggested that degradation of nitramines in sterilized natural coastal waters, away from light, was mainly governed by alkaline hydrolysis. Kinetic calculations using the present parameters showed that alkaline hydrolysis of RDX and HMX in marine waters at 10 degrees C would respectively take 112 +/- 10 and 2408 +/- 217 yr to be completed (99.0%). We concluded that under natural conditions hydrolysis should not contribute significantly to the natural attenuation of HMX in coastal waters whereas it could play an active role in the natural attenuation of RDX.     

Measured concentrations of herbicides and model predictions of atrazine fate in the Patuxent River estuary

The environmental fate of herbicides in estuaries is poorly understood. Estuarine physical transport processes and the episodic nature of herbicide release into surface waters complicate interpretation of water concentration measurements and allocation of sources. Water concentrations of herbicides and two triazine degradation products (CIAT [6-amino-2-chloro-4-isopropylamino-s-triazine] and CEAT [6-amino-2-chloro-4-ethylamino-s-triazine]) were measured in surface water from four sites on 40 d from 4 Apr. through 29 July 19% in the Patuxent River estuary, part of the Chesapeake Bay system. Atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine) was most persistent and present in the highest concentrations (maximum = 1.29 microg/L). Metolachlor [2-chloro-6'-ethyl-N-(2-methoxy-1-methylethyl)-o-acetoluidide], CIAT, CEAT, and simazine (1-chloro-3,5-bisethylamino-2,4,6-triazine) were frequently detected with maximum concentration values of 0.61, 1.1, 0.76, and 0.49 microg/L, respectively. A physical transport model was used to interpret atrazine concentrations in the context of estuarine water transport, giving estimates of in situ degradation rates and total transport. The estimated half-life of atrazine in the turbid, shallow upper estuary was t(1/2) = 20 d, but was much longer (t(1/2) = 100 d) in the deeper lower estuary. Although most (93%) atrazine entered the estuary upstream via the river, simulations suggested additional inputs directly to the lower estuary. The total atrazine load to the estuary from 5 April to 15 July was 71 kg with 48% loss by degradation and 31% exported to the Chesapeake Bay. Atrazine persistence in the estuary is directly related to river flows into the estuary. Low flows will increase atrazine residence time in the upper estuary and increase degradation losses.     

ANALYSIS OF HYDRILLA-INHIBITING FRACTIONS IN NATURAL WATERS: THE CONCEPT OF “FINGERPRINTING” THROUGH LIQUID CHROMATOGRAPHY1

ABSTRACT: High performance liquid chromatography (HPLC) has been used to identify a fraction of aqueous sediment extract from Lake Starvation, Hillsborough County, Florida, that is responsible for inhibition of hydrilla growth. The fraction was separated on a Zorbax? C₁₈ preparative-scale column. The present study examines various lake sediment extracts and river water samples to determine the presence or absence of the inhibitor peak. The biologically active component is absent in certain rivers where hydrilla is prominent, but it is present in extracts of Lake Starvation and White Trout Lake sediments that are known to have hydrilla growth inhibiting properties. The implications of “fingerprinting” natural waters for hydrilla inhibitor through liquid chromatography are considered.     

Spatiotemporal Variability in Water Sources Controls Chemical and Physical Properties of a Semi‐arid Urban River System

We conducted synoptic surveys over three seasons in one year to evaluate the variability in water sources and geochemistry of an urban river with complex water infrastructure in the state of Utah. Using stable isotopes of river water (δ¹⁸O and δ²H) within a Bayesian mixing model framework and a separate hydrologic mass balance approach, we quantified both the proportional inputs and magnitude of discharge associated with “natural” (lake, groundwater, and tributary inputs) and “engineered” (effluent and canal inflows) sources. The relative importance of these major contributors to streamflow varied both spatially and seasonally. Spatiotemporal patterns of dissolved oxygen, temperature, pH, calcium, chloride, nitrate, and orthophosphate indicated seasonal shifts in dominant sources of river water played an important role in determining water quality. We show although urban rivers are clearly influenced by novel water sources created by water infrastructure, they continue to reflect the imprint of “natural” water sources, including diffuse groundwater. Resource managers thus may need to account for the quantity of both surface waters and also historically overlooked groundwater inputs to address water quality concerns in urban rivers.     

Herbicide and nutrient transport from an irrigation district into the South Saskatchewan River

Pesticides and nutrients can be transported from treated agricultural land in irrigation runoff and thus can affect the quality of receiving waters. A 3-yr study was carried out to assess possible detrimental effects on the downstream water quality of the South Saskatchewan River due to herbicide and plant nutrient inputs via drainage water from an irrigation district. Automated water samplers and flow monitors were used to intensively sample the drainage water and to monitor daily flows in two major drainage ditches, which drained approximately 40% of the flood-irrigated land within the irrigation district. Over three years, there were no detectable inputs of ethalfluralin into the river and those of trifluralin were less than 0.002% of the amount applied to flood-irrigated fields. Inputs of MCPA, bromoxynil, dicamba and mecoprop were 0.06% or less of the amounts applied, whereas that for clopyralid was 0.31%. The relatively higher input (1.4%) of 2,4-D to the river was probably due its presence in the irrigation water. Corresponding inputs of P (as total P) and N (as nitrate plus ammonia) were 2.2 and 1.9% of applied fertilizer, respectively. Due to dilution of the drainage water in the river, maximum daily herbicide (with the exception of 2,4-D) and nutrient loadings to the river would not have resulted in significant concentration increases in the river water. There was no consistent remedial effect on herbicides entering the river due to passage of the drainage water through a natural wetland. In contrast, a considerable portion of the nutrients entering the river originated from the wetland.     

Soil chemical changes resulting from irrigation with water co-produced with coalbed natural gas

Land application of coalbed natural gas (CBNG) co-produced water is a popular management option within northwestern Powder River Basin (PRB) of Wyoming. This study evaluated the impacts of land application of CBNG waters on soil chemical properties at five sites. Soil samples were collected from different depths (0-5, 5-15, 15-30, 30-60, 60-90, and 90-120 cm) from sites that were irrigated with CBNG water for 2 to 3 yr and control sites. Chemical properties of CBNG water used for irrigation on the study sites indicate that electrical conductivity of CBNG water (EC(w)) and sodium adsorption ratio of CBNG water (SAR(w)) values were greater than those recommended for irrigation use on the soils at the study sites. Soil chemical analyses indicated that electrical conductivity of soil saturated paste extracts (EC(e)) and sodium adsorption ratio of soil saturated paste extracts (SAR(e)) values for irrigated sites were significantly greater (P < 0.05) than control plots in the upper 30-cm soil depths. Mass balance calculations suggested that there has been significant buildup of Na in irrigated soils due to CBNG irrigation water as well as Na mobilization within the soil profiles. Results indicate that irrigation with CBNG water significantly impacts certain soil properties, particularly if amendments are not properly utilized. This study provides information for better understanding changes in soil properties due to land application of CBNG water. These changes must be considered in developing possible criteria for preserving fragile PRB ecosystems.     

Pesticide fate and transport throughout unsaturated zones in five agricultural settings, USA

Pesticide transport through the unsaturated zone is a function of chemical and soil characteristics, application, and water recharge rate. The fate and transport of 82 pesticides and degradates were investigated at five different agricultural sites. Atrazine and metolachlor, as well as several of the degradates of atrazine, metolachlor, acetochlor, and alachlor, were frequently detected in soil water during the 2004 growing season, and degradates were generally more abundant than parent compounds. Metolachlor and atrazine were applied at a Nebraska site the same year as sampling, and focused recharge coupled with the short time since application resulted in their movement in the unsaturated zone 9 m below the surface. At other sites where the herbicides were applied 1 to 2 yr before sampling, only degradates were found in soil water. Transformations of herbicides were evident with depth and during the 4-mo sampling time and reflected the faster degradation of metolachlor oxanilic acid and persistence of metolachor ethanesulfonic acid. The fraction of metolachlor ethanesulfonic acid relative to metolachlor and metolachlor oxanilic acid increased from 0.3 to >0.9 at a site in Maryland where the unsaturated zone was 5 m deep and from 0.3 to 0.5 at the shallowest depth. The flux of pesticide degradates from the deepest sites to the shallow ground water was greatest (3.0-4.9 micromol m(-2) yr(-1)) where upland recharge or focused flow moved the most water through the unsaturated zone. Flux estimates based on estimated recharge rates and measured concentrations were in agreement with fluxes estimated using an unsaturated-zone computer model (LEACHM).     

Studies on the effect of Bladex and Etazine on bacterial indices of pollution

The effect of the triazine herbicides Etazine and Bladex on coliform and fecal streptococci groups was studied in Nile river water, Nile water seeded with sewage, and autoclaved Nile water. The results indicate the fecal streptococci were able to persist and multiply in Nile water containing Bladex or Etazine and seeded with sewage. The successive addition of Bladex and Etazine (up to 10 mg/liter) increased its degradation rate and had no inhibitory effect on the bacterial parameters.     

Are intensive agricultural practices environmentally and ethically sound?

Soil is fragile and nonrenewable but the most basic of natural resources. It has a capacity to tolerate continuous use but only with proper management. Improper soil management and indiscriminate use of chemicals have contributed to some severe global environmental issues, e.g., volatilization losses and contamination of natural waters by sediments and agricultural fertilizers and pesticides. The increasing substitution of energy for labor and other cultural inputs in agriculture is another issue. Fertilizers and chemicals account for about 25% of the production energy investment in agriculture. An additional 60% is accounted for by machinery, gasoline, electricity, and power-related inputs. Fertilizer additions to cropland are not utilized fully and significant amounts, depending on conditions, are either lost in surface runoff or leached into the ground water. The annual discharge of dissolved solids from agricultural lands to the waterways in the USA is substantial. The increasing use of herbicides in agriculture is a threat to the quality of surface and ground water, although this threat is dependent upon both the chemistry of the compound and the ecosystem in which it is used. Especially within the Third World, development of an environmental ethic and environmental laws have not kept pace with the increase in pesticide use. Above all is the severe and global problem of soil degradation currently occurring at the rate of five to seven million hectares per year. The policy and moral aspects of these issues are discussed.     

Runoff and drainage losses of atrazine, metribuzin, and metolachlor in three water management systems

Rainfall can transport herbicides from agricultural land to surface waters, where they become an environmental concern. Tile drainage can benefit crop production by removing excess soil water but tile drainage may also aggravate herbicide and nutrient movement into surface waters. Water management of tile drains after planting may reduce tile drainage and thereby reduce herbicide losses to surface water. To test this hypothesis we calculated the loss of three herbicides from a field with three water management systems: free drainage (D), controlled drainage (CD), and controlled drainage with subsurface irrigation (CDS). The effect of water management systems on the dissipation of atrazine (6-chloro-N2-ethyl-N4-isopropyl-1,3,5-triazine-2,4-diamine), metribuzin [4-amino-6-(1,1-dimethylethyl)-3-(methylthio)-1,2,4-triazine-5(4H)-one), and metolachlor [2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide] in soil was also monitored. Less herbicide was lost by surface runoff from the D and CD treatments than from CDS. The CDS treatment increased surface runoff, which transported more herbicide than that from D or CD treatments. In one year, the time for metribuzin residue to dissipate to half its initial value was shorter for CDS (33 d) than for D (43 d) and CD (46 d). The half-life of atrazine and metolachlor were not affected by water management. Controlled drainage with subsurface irrigation may increase herbicide loss through increased surface runoff when excessive rain is received soon after herbicide application. However, increasing soil water content in CDS may decrease herbicide persistence, resulting in less residual herbicide available for aqueous transport.     

Environmental concentrations of agricultural herbicides: 2,4-d and triallate

The herbicides 2,4-D (2,4-dichlorophenoxyacetic acid) and triallate [S-2,3,3-trichloroallyl di-isopropyl(thiocarbamate)] are extensively used to control broadleaf and wild oat (respectively) weed infestations in Canadian cereal crops. In 1990, for example, more than 3.8 million kg of 2,4-D and 2.7 million kg of triallate were applied in the three prairie provinces (Alberta, Saskatchewan, and Manitoba). Maximum air concentrations of these two herbicides during the summers of 1989 and 1990 near Regina, Saskatchewan, were 3.90 ng m(-3) (2,4-D) and 60.04 ng m(-3) (triallate). Concentrations of these two herbicides were also measured in bulk atmospheric deposition (wet plus dry) and in farm pond water and associated surface film. Maximum measured levels of 2,4-D were 3550 ng m(-2) d(-1) (bulk deposition), 332 ng m(-2) (surface film), and 290 ng L(-1) (pond water). Maximum levels of triallate were 2300 ng m(-2) d(-1) (bulk deposition), 212 ng m(-2) (surface film), and 500 ng L(-1) (pond water). The highest quantities of the herbicides tended to be found during or immediately after the time of regional application. The movement of the herbicides in the environment will be discussed in relation to the four matrices studied.     

Evaluation of water quality in the Ouémé River (Bénin)

Water is an essential element for humankind, animals, and plants. It is also an important element of the aquatic environment (the natural habitat of multiple species), where its quality plays a determining role in their protection and conservation. Unfortunately, the water quality of natural environments has worsened in the last decades. In sub-Saharan Africa and particularly in Bénin, in contrast to river discharges, monitoring the quality of surface water is a very rare activity. Thus, knowledge about physical and chemical properties as a basis for evaluation of the state of the environment and protection measures needed is almost absent. This article presents the results of the first structured, regular monitoring campaign on surface waters in the whole basin of the Ouémé River in Bénin Republic. With 510 km, the Ouémé River’s water quality fluctuates from upstream (Taneka Koko mountains in the north) to downstream (gauging station Bonou in the south) sources. This is due to soil erosion, lack of water treatment plants, and the use of significant quantities of fertilizer in the cotton zone. The present research was initiated to study the resource degradation of this area through chemical and physical water analysis. The monitoring of water quality has been followed for 5 years on twenty physicochemical parameters, from samples taken at four gauging stations on the main channel of the Ouémé River. Means and standard deviations of water analysis results were compared to both the recommendations of the World Health Organization (WHO) and the Maximum Permissible Concentrations (MPC) for drinking water (WHO 1987). Thus, high values were observed for physical parameters, i.e., color and turbidity had peaks of 697.5 uC and 129 FTU at Bétérou station in the wet season, although certain parameters, such as total hardness, present low values compared to the recommended standards. Moreover, excluding the concentrations of NO₂ ⁻ and NH₄ ⁺ with values above the MPC, nutrient concentrations posed no direct risk for human consumption. However, together with phosphate concentrations (which are up to ten times higher than permissible ecological thresholds), they can cause eutrophication of the aquatic ecosystem. Due to the current flow regime, which has very low discharge rates in the dry season and torrential rainfall and high sediment loads in the wet season, the risk of eutrophication, i.e., excessive concentrations of ammonium and phosphates, is present throughout the year. Accumulation of ammonium and the distribution of nitrate and nitrites in the river water suggest that nitrification is impeded due to a lack of oxygen in both dry and wet seasons. Finally, the investigations show that the risk of water pollution exists and it is necessary to take measures of sanitation and water treatment to prevent the further degradation of water along the Ouémé River.     

基于流域视角的水环境综合治理规划研究——以江苏省淀山湖为例

以流域为单元进行水资源综合规划和管理是实现水环境改善的重要途径。本文以太湖流域第二大省界湖泊—淀山湖为例,在综合分析流域水环境质量基础上,利用GIS 分析工具划分流域治理片区并制定分区管控策略。根据流域所含骨干河流流向、骨干河流与淀山湖交汇特点、上中下游不同河段及镇域行政边界,将淀山湖流域分为吴淞江流域、千灯浦- 淀山湖流域、昆南湖荡流域、元荡湖荡流域、太浦河流域五大片区138 个子评价单元。通过水环境容量与压力两类空间叠加分析,构建形成污染重点减排区、污染综合治理区、产业绿色化提升区、生态环境保育区等四个类型区域,并提出差异化的产业准入和环境治理措施。本研究不仅为以流域为治理单元的水环境治理规划提供了较为可行的技术体系,而且为太湖流域水环境综合整治思路创新提供了可借鉴的案例。     

Lake eutrophication management modeling using dynamic programming

Lake eutrophication problems have received considerable attention in Taiwan, especially because they relate to the quality of drinking water. In this study, steady-state river water quality and lake eutrophication models are solved using dynamic programming algorithms to find the nutrient removal rates for eutrophication control during dry season. The kinetic cycle of chlorophyll-a, phosphorus and nitrogen for a complete-mixed lake is considered in the optimization framework. The Newton-iterative technique is adopted to solve the nonlinear equations for the steady-state lake eutrophication model. The optimization framework is applied to Cheng-Ching Lake in southern Taiwan. Several nutrient loading scenarios for eutrophication control are studied. Optimization results for nutrient removal rates and corresponding wastewater treatment capacities of each reach of the Kao-Ping River define the least cost approach to lake eutrophication control. A natural purification method, structural free water surface wetland, is also suggested to save more investment and improve river water quality at the same time.     

Combined use of GIS and environmental indicators for assessment of chemical, physical and biological soil degradation in a Spanish Mediterranean region

Soil is one of the main non-renewable natural resources in the world. In the Valencian Community (Mediterranean coast of Spain), it is especially important because agriculture and forest biomass exploitation are two of the main economic activities in the region. More than 44% of the total area is under agriculture and 52% is forested. The frequently arid or semi-arid climate with rainfall concentrated in few events, usually in the autumn and spring, scarcity of vegetation cover, and eroded and shallow soils in several areas lead to soil degradation processes. These processes, mainly water erosion and salinization, can be intense in many locations within the Valencian Community. Evaluation of soil degradation on a regional scale is important because degradation is incompatible with sustainable development. Policy makers involved in land use planning require tools to evaluate soil degradation so they can go on to develop measures aimed at protecting and conserving soils. In this study, a methodology to evaluate physical, chemical and biological soil degradation in a GIS-based approach was developed for the Valencian Community on a 1/200,000 scale. The information used in this study was obtained from two different sources: (i) a soil survey with more than 850 soil profiles sampled within the Valencian Community, and (ii) the environmental information implemented in the Geo-scientific map of the Valencian Community digitised on an Arc/Info GIS. Maps of physical, chemical and biological soil degradation in the Valencian Community on a 1/200,000 scale were obtained using the methodology devised. These maps can be used to make a cost-effective evaluation of soil degradation on a regional scale. Around 29% of the area corresponding to the Valencian Community is affected by high to very high physical soil degradation, 36% by high to very high biological degradation, and 6% by high to very high chemical degradation. It is, therefore, necessary to draw up legislation and to establish the policy framework for actions focused on preventing soil degradation and conserving its productive potential.     

REGRESSION MODELS OF HERBICIDE CONCENTRATIONS IN OUTFLOW FROM RESERVOIRS IN THE MIDWESTERN USA, 1992–19931

ABSTRACT: Reservoirs are used to store water for public water supply, flood control, irrigation, recreation, hydropower, and wildlife habitat, but also often store undesirable substances such as herbicides. The outflow from 76 reservoirs in the midwestern USA, was sampled four times in 1992 and four times in 1993. At least one herbicide was detected in 82.6 percent of all samples, and atrazine was detected in 82.1 percent of all samples. Herbicide properties; topography, land use, herbicide use, and soil type in the contributing drainage area; residence time of water in reservoirs; and timing of inflow, release, and rainfall all can affect the concentration of herbicides in reservoirs. A GIS was used to quantify characteristics of land use, agricultural chemical use, climatic conditions, topographic character, and soil type by reservoir drainage basins. Multiple linear and logistic regression equations were used to model mean herbicide concentrations in reservoir outflow as a function of these characteristics. Results demonstrate a strong association between mean herbicide concentrations in reservoir outflow and herbicide use rates within associated drainage basins. Results also demonstrate the importance of including soils and basin hydrologic characteristics in models used to estimate mean herbicide concentrations.     

聚丙烯酰胺化学降解技术研究进展

聚丙烯酰胺化学降解技术是目前油田含聚污水处理的重要技术之一,包括氧化降解法、光降解法和光催化降解法。文章介绍了此项技术在降解机理和应用方面的研究进展,并通过实验证明了聚丙烯酰胺氧化降解和光降解的可行性,对油田污水中聚丙烯酰胺的化学降解处理具有一定的指导意义。