Effect of Cellulose/Hemicellulose and Lignin on the Bioavailability of Toluene Sorbed to Waste Paper

140

122

The non-Aroclor congener 3,3'-dichlorobiphenyl (PCB 11) has been recently detected in air, water, biota, sediment, and suspended sediment. Although it has been known since at least the 1970s that this congener is produced inadvertently during the production of diarylide yellow pigments, this work presents the first evidence that the use of these pigments in consumer goods results in the dispersion of PCB 11 throughout the environment at levels that are problematic in terms of achieving water quality standards for the sum of polychlorinated biphenyls (PCBs). In this work, PCB 11 is measured at ppb levels in consumer goods that are likely to be discarded in ways that allow them to enter wastewater treatment plants and combined sewer overflows, including newspapers, magazines, cardboard boxes used for food packaging, and plastic bags. Also, using data sets acquired for the purpose of calculating total maximum daily loads (TMDLs) for PCBs, PCB 11 loads to the New York/New Jersey Harbor and Delaware River are calculated. Despite the fact that there are no known manufacturers of diarylide yellow pigments in the Delaware River watershed, the loads of PCB 11 to the Delaware River exceed the TMDL for the sum of PCBs by nearly a factor of 2. The ratio of PCB 11 to a characteristic dechlorination end product, PCB 4 (2,2'-dichlorobiphenyl), in these data sets indicates that dechlorination is not a significant source of PCB 11 in these systems. In the upper Hudson River, where extensive dechlorination of heavy PCB congeners occurs, the ratio is just 0.012. In contrast, downstream in the NY/NJ Harbor as well as in the Delaware River the ratio is much higher and more variable. Pigment use therefore appears to be the main source of PCB 11 in these systems, and this congener is likely to present a significant obstacle to achieving PCB water quality standards throughout the United States.

Section: Resultsmentioning

confidence: 99%

Evidence for Unique and Ubiquitous Environmental Sources of 3,3′-Dichlorobiphenyl (PCB 11)

Rodenburg

Guo

et al. 2009

140

122

“…As a type of polysaccharide, cellulose is the most abundant organic compound on earth synthesized primarily in plants . Lignin is also a natural component of plants, presenting in large quantities in cell walls of plants. , Both lignin and cellulose are major components of paper, which is the largest source of municipal solid waste, leading them the most abundant organic matter in landfills. Additionally, cellulose and lignin are ubiquitous biopolymers in the environment and precursors of SOMs .…”

Section: Methodsmentioning

confidence: 99%

Impact of the Simulated Diagenesis on Sorption of Naphthalene and 1-Naphthol by Soil Organic Matter and its Precursors

Guo

Wang

Zhou

et al. 2013

Soil organic matter (SOM) in a peat soil, humic acid, and humin and their precursors (i.e., cellulose and lignin) were treated at high temperature (250 and 400 °C) with high pressure in a sealed platinum reaction kittle to simulate the influence of diagenesis on their composition and structure, and impact of the simulated diagenesis on sorption behaviors of hydrophobic organic compounds (HOCs) (i.e., naphthalene and 1-naphthol) by these samples was investigated. High temperature and pressure treatment greatly influenced chemical composition and physical properties of the original samples and their sorption for both naphthalene and 1-naphthol. Sorption of naphthalene by all samples was jointly regulated by hydrophobic and π-π interactions with their alkyl and aromatic carbon moieties, which was derived from the positive correlation between total hydrophobic carbon content of all sorbents and their organic carbon content-normalized sorption coefficients (Koc) for this compound (p = 0.075). However, sorption of 1-naphthol by the tested sorbents was governed by hydrogen bonding with their O-containing polar functionalities, as derived from the positive correlation between Koc values of 1-Naph and their polarity index ((O+N)/C). Difference in sorption mechanisms of naphthalene and 1-naphthol by the original and treated samples noted the great influence of chemical composition of sorbates on their interaction and essential roles of specific interactions (e.g., hydrogen bonding) in sorption of polar compound (i.e., 1-naphthol) to these sorbents. Surface area (SA) and porosity data of sorbents obtained from N2 sorption-desorption isotherms at 77 K showed that new SA and pores were created during the diagenetic process of all original samples, which provided substantial sorption sites and thus enhanced sorption of naphthalene and 1-naphthol. Among all tested samples, physicochemical properties of cellulose were most strongly affected by the simulated diagenetic process, and impact of such a process on its sorption intensity for the tested compounds was the most significant. The characterization data of the treated sorbents showed that the high temperature and pressure treatment similarly simulated the naturally occurring diagenesis of SOMs and their precursors, which is a first attempt. These findings are valuable for better understanding of the sorption behaviors of HOCs to SOM and its precursors as affected by diagenesis, which in turn is critical for elucidating the transport and fate of HOCs in the environment.

“…Besides the abundance in crops/plants, cellulosic substances also form a large fraction of waste-paper products disposed at various municipal landfill sites (9). This situation raises a concern for whether these substances strongly retain certain organic contaminants and thus influence their transport and fate.…”

Section: Introductionmentioning

confidence: 99%

Partition Coefficients of Organic Contaminants with Carbohydrates

Hung

Lin

Chiou

2010

In view of the current lack of reliable partition coefficients for organic compounds with carbohydrates (K ch ), carefully measured values with cellulose and starch, the two major forms of carbohydrates, are provided for a wide range of compounds: short-chain chlorinated hydrocarbons, halogenated benzenes, alkyl benzenes, polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls, and organochlorine pesticides. To ensure the accuracy of the K ch data, solute concentrations in both water and carbohydrate phases are measured by direct solvent extraction of the samples. For a given compound, the observed partition coefficient with cellulose (K cl ) is virtually the same as that with starch (K st ). This finding expedites the evaluation of organic contamination with different forms of carbohydrates. The presently determined K ch values of 13 PAHs are substantially lower (by 3-66 times) than the literature data; the latter are suspect as they were obtained with (i) presumably impure carbohydrate samples or (ii) indirectly measured equilibrium solute concentrations in carbohydrate and water phases. Although the K ch values are generally considerably lower than the respective K ow (octanol-water) or K lipid (lipid-water), accurate K ch data are duly required to accurately estimate the contamination of carbohydrates by organic compounds because of the abundance of carbohydrates over lipids in crops and plants. To overcome the current lack of reliable K ch data for organic compounds, a close correlation of log K ch with log K ow has been established for predicting the unavailable K ch data for low-polarity compounds.