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Organosolv treatment is an environmentally friendly fractionation method that affords a lignin stream with high purity. The severity of the treatment affects the chemical composition of the generated, very complex lignin degradation product mixtures. Understanding the effects of the process severity on the types and relative abundances of the individual compounds in the mixtures is of great importance for the optimization of the treatment and the development of downstream conversion processes. In this study, seven organosolv switchgrass lignin samples prepared at different reaction temperatures and using different acid concentrations and reaction times were initially analyzed by using high-resolution mass spectrometry with negative ion-mode electrospray ionization ((−)ESI HRMS). Fast pyrolysis coupled with negative ion-mode atmospheric pressure chemical ionization and HRMS (py/(−)APCI HRMS) was also used to characterize the lignin degradation products. This method generated similar data as (−)ESI HRMS. Lignin monomers and dimers were found to constitute the majority of compounds in the mixtures. High-performance liquid chromatography coupled with (−)ESI high-resolution multistage tandem mass spectrometry (HPLC/(−)ESI HRMSn) based on collision-activated dissociation (CAD) was employed to obtain structural information for the most abundant compounds as well as a β-O-4 dimer with a relatively low abundance in the organosolv lignin samples. The relative abundances of lignin–carbohydrate complexes were found to be high under mild organosolv treatment conditions but become low under moderate and harsh treatment conditions. As lignin compounds with β-O-4 linkages are not stable under acidic conditions, the relative abundances of these compounds were found to be very low. The relative amounts of lignin monomers decreased as the treatment severity increased while the relative abundances of lignin dimers, trimers, and bigger oligomers increased, possibly due to repolymerization reactions under the harsher treatment conditions.

Release of microplastics (MPs) and nanoplastics (NPs) into agricultural fields is of great concern due to their reported ecotoxicity to organisms that provide beneficial service to the soil such as earthworms, and the potential ability of MPs and NPs to enter the food chain. Most fundamental studies of the fate and transport of plastic particulates in terrestrial environments employ idealized MP materials as models, such as monodisperse polystyrene spheres. In contrast, plastics that reside in agricultural soils consist of polydisperse fragments resulting from degraded films employed in agriculture. There exists a need for more representative materials in fundamental studies of the fate, transport, and ecotoxicity of MPs and NPs in soil ecosystems. The objective of this study was therefore to develop a procedure to produce MPs and NPs from agricultural plastics (a mulch film prepared biodegradable polymer polybutyrate adipate-co-terephthalate (PBAT) and low-density PE [LDPE]), and to characterize the resultant materials. Soaking of PBAT films under cryogenic conditions promoted embrittlement, similar to what occurs through environmental weathering. LDPE and cryogenically-treated PBAT underwent mechanical milling followed by sieve fractionation into MP fractions of 840 μm, 250 μm, 106 μm, and 45 μm. The 106 μm fraction was subjected to wet grinding to produce NPs of average particle size 366.0 nm and 389.4 nm for PBAT and LDPE, respectively. A two-parameter Weibull model described the MPs' particle size distributions, while NPs possessed bimodal distributions. Size reduction did not produce any changes in the chemical properties of the plastics, except for slight depolymerization and an increase of crystallinity resulting from cryogenic treatment. This study suggests that MPs form from cutting and high-impact mechanical degradation as would occur during the tillage into soil, and that NPs form from the MP fragments in regions of relative weakness that possess lower molecular weight polymers and crystallinity.

Terrestrial nanoplastics (NPs) pose a serious threat to agricultural food production systems due to the potential harm of soil-born micro- and macroorganisms that promote soil fertility and ability of NPs to adsorb onto and penetrate into vegetables and other crops. Very little is known about the dispersion, fate and transport of NPs in soils. This is because of the challenges of analyzing terrestrial NPs by conventional microscopic techniques due to the low concentrations of NPs and absence of optical transparency in these systems. Herein, we investigate the potential utility of small-angle neutron scattering (SANS) and Ultra SANS (USANS) to probe the agglomeration behavior of NPs prepared from polybutyrate adipate terephthalate, a prominent biodegradable plastic used in agricultural mulching, in the presence of vermiculite, an artificial soil. SANS with the contrast matching technique was used to study the aggregation of NPs co-dispersed with vermiculite in aqueous media. We determined the contrast match point for vermiculite was 66% D2O / 33% H2O. At this condition, the signal for vermiculite was ~50-100%-fold lower that obtained using neat H2O or D2O as solvent. According to SANS and USANS, smaller-sized NPs (50 nm) remained dispersed in water and did not undergo size reduction or self-agglomeration, nor formed agglomerates with vermiculite. Larger-sized NPs (300-1000 nm) formed self-agglomerates and agglomerates with vermiculite, demonstrating their significant adhesion with soil. However, employment of convective transport (simulated by ex situ stirring of the slurries prior to SANS and USANS analyses) reduced the self-agglomeration, demonstrating weak NP-NP interactions. Convective transport also led to size reduction of the larger-sized NPs. Therefore, this study demonstrates the potential utility of SANS and USANS with contrast matching technique for investigating behavior of terrestrial NPs in complex soil systems.

Lignin, a low value by-product of biomass fractionation, is of current particular interest for the production of value added materials such as carbon fibers within a biorefinery. Accordingly, we have isolated lignin, hemicellulose, and cellulose by organosolv fractionation of loblolly pine (Pinus taeda) under the influence different fractionation severities (2.50–3.31). A designed experimental matrix targeted maximum lignin and pulp yields and lignin glass transition temperature (Tg) as a function of several process parameters. Optimal fractionation conditions were estimated from an enhanced regression model of the statistically significant variables generated using response surface design (RSD). The most significant factor influencing lignin and pulp yields was solvent composition (p-value