Joseph Lichwa

A comparison of liquid hot water and steam pretreatments of sugar cane bagasse for bioconversion to ethanol

Sugar cane bagasse was pretreated with either liquid hot water (LHW) or steam using the same 25 l reactor. Solids concentration ranged from 1% to 8% for LHW pretreatment and was > or = 50% for steam pretreatment. Reaction temperature and time ranged from 170 to 230 degrees C and 1 to 46 min, respectively. Key performance metrics included fiber reactivity, xylan recovery, and the extent to which pretreatment hydrolyzate inhibited glucose fermentation. In four cases, LHW pretreatment achieved > or = 80% conversion by simultaneous saccharification and fermentation (SSF). > or = 80% xylan recovery, and no hydrolyzate inhibition of glucose fermentation yield. Combined effectiveness was not as good for steam pretreatment due to low xylan recovery. SSF conversion increased and xylan recovery decreased as xylan dissolution increased for both modes. SSF conversion, xylan dissolution. hydrolyzate furfural concentration, and hydrolyzate inhibition increased, while xylan recovery and hydrolyzate pH decreased, as a function of increasing LHW pretreatment solids concentration (1-8%). These results are consistent with the notion that autohydrolysis plays an important. if not exclusive, role in batch hydrothermal pretreatment. Achieving concurrently high (greater than 90%) SSF conversion and xylan recovery will likely require a modified reactor configuration (e.g. continuous percolation or base addition) that better preserves dissolved xylan.

The fate and transport of RDX, HMX, TNT and DNT in the volcanic soils of Hawaii: a laboratory and modeling study.

The adsorption and degradation behavior of RDX, HMX, TNT and DNT and the impact of pH, ionic strength and dissolved organic matter on sorption were examined for two volcanic soils of a former military training area on Hawaii Island, Hawaii, USA. The transport of these chemicals in the soil was also studied in small packed columns and simulated using a water-flow and solute-transport model, HYDRUS_1D. The results show that HMX and RDX are both significantly more mobile than TNT and DNT. The adsorbability of the four chemicals was ranked as: RDXRDX>DNT>TNT. No significant trend was observed for the effect of ionic strength, pH and dissolved organic carbon (DOC) on the adsorption of explosive compounds within the concentrations and pH ranges evaluated. The simulation results show that TNT and DNT would not leach beyond a depth of 30cm soil profile whereas a significant amount of HMX and RDX would pass the 30cm depth. It seems that the risk for contamination of groundwater is much higher for both HMX and RDX than for DNT and TNT as the substratum in this area consists of highly permeable lavas.

Fate and transport of TNT, RDX, and HMX in streambed sediments: implications for riverbank filtration.

Riverbank filtration (RBF) refers to the process of capturing surface water passing through the river-sediment-aquifer system by using a collection technique such as a well or an infiltration gallery. RBF removes nearly all suspended and a large number of dissolved contaminants from the surface water. Therefore, it can function as an effective pretreatment process in drinking-water production. TNT (2,4,6-trinitrotoluene), RDX (1,3,5-trinitro-1,3,5-triazacyclohexane), and HMX (1,3,5,7-tetranitro-1,3,5,7-tetrazocane) are three military explosive chemicals that are considered of concern to human health when present in source waters. This study is to evaluate the ability of the filtration media in RBF systems to remove these chemicals. The results from an anoxic batch test showed that all three chemicals will degrade while passing through streambed sediments. The pseudo first-order degradation-rate constants for TNT, RDX, and HMX were measured to be 0.33, 0.055, and 0.033d(-1), respectively. Under aerobic conditions only TNT showed significant degradation. Results from a model RBF system showed that the mobility of the three chemical contaminants in streambed sediments was in the order: HMX>RDX>TNT. The results suggest that RBF is capable of removing TNT and RDX but HMX levels may continue to be of concern-especially when collector wells use laterals running directly beneath the stream or riverbed.

Impact of different land uses on polycyclic aromatic hydrocarbon contamination in coastal stream sediments.

PAHs are ubiquitous environmental pollutants that can cause adverse health and ecological effects. In the present study, we examined the impact of land use on the concentration and composition of PAHs in 28 coastal stream sediments on the Island of Oahu, Hawaii. In densely populated urban areas, the concentration range of total PAHs in the stream sediments affected by mixed residential and industrial activities (RI) are 0.40-9.05 ppm, which is significantly higher than the 0.36-4.21 ppm detected in the stream sediments affected predominantly by urban residential land uses (UR). The stream sediments affected by agricultural activities (AG) reported a concentration range of 0.09-2.14 ppm, which is lower than those of the RI and UR stream sediments. The molecular weight of PAH is a factor, as only high molecular weight (HMW) PAHs were significantly affected by land uses (ANOVA P=0.009). Correlation analysis showed that only in the UR stream sediments were significant correlations observed between PAH concentration and two anthropogenic indicators: population density (r=0.57, P=0.027) and vehicle density (r=0.55, P=0.034). The fractional concentrations of PAHs were analyzed by using PCA analysis, which led to the separate clustering of the RI and AG stream sediments and suggest distinct PAH sources between the two land uses. Two PAH source indicators, including Ant/(Ant+Phe) and Fl/(Fl+Py), indicates that PAHs sources in the RI stream sediments are most likely of petroleum origin, while PAHs in the UR and AG stream sediments most likely came from combustion activities. In addition, the concentration and relative potency of carcinogenic PAHs in the coastal stream sediments exhibited similar patterns as the total PAH concentration with respect to land uses.

Fate and transport of selected estrogen compounds in Hawaii soils: Effect of soil type and macropores

The fate and transport of estrogen compounds in the environment is of increasing concern due to their potential impact on freshwater organisms, ecosystems and human health. The behavior of these compounds in batch experiments suggests low mobility, while field studies indicate the persistence of estrogen compounds in the soil with the possibility of migration to surface water as well as groundwater. To better understand the movement of these chemicals through soils, we examined their transport in three different Hawaiian soils and two aqueous matrices. The three different soils used were an Oxisol, a Mollisol and a cinder, characterized by different mineralogical properties and collected at depths of 60-90 cm and 210-240 cm. Two liquid matrices were used; deionized (DI) water containing calcium chloride (CaCl2), and recycled water collected from a wastewater treatment facility. The experiments were conducted in packed and structured columns. Non-equilibrium conditions were observed during the study, especially in the structured soil. This is believed to be primarily related to the presence of macropores in the soil. The presence of macropores resulted in reduced contact time between soil and estrogens, which facilitated their transport. We found that the organic carbon content and mineralogical composition of the soils had a profound effect on the transport of the estrogens. The mobility of estrone (E1) and 17β-estradiol (E2) was greater in cinder than in the other soils. In column experiments with recycled water, earlier breakthrough peaks and longer tails of estrogens were produced compared to those observed using DI water. The use of recycled water for agricultural purposes and the siting of septic tanks and cesspools should be critically reviewed in light of these findings, especially in areas where groundwater is the primary source of potable water, such as Hawaii.

Essential Oils of Selected Hawaiian Plants and Associated Litters

Abstract The chemical composition of the essential oils from the leaves of Araucaria heterophylla (also known as Norfolk Island pine), Casuarina cunninghamian, Eucalyptus citriodora, Psidium cattlenium var. lucidum (also known as strawberry guava), and litters of the first two species were studied using two gas chromatography techniques, one equipped with a mass spectrometer detector (GC/MS) and the other with a fame ionization detector (GC/FID). Six volatile compounds were identified in the leaf oil of A. heterophylla. A substantial increase in the amount of α-pinene, α-terpinene and a decrease in the amount of β-caryophyllene was noticed in the litter oil of A. heterophylla. Three volatile compounds were identifed in C. cunninghamian. Another monoterpene, α-terpinene, was observed in the litter oil of C. cunninghamian. Eleven compounds were identified in the leaf oil of P. cattlenium, of which β-caryophyllene (59.0%), α-pinene (13.2%) and myrcene (11.3%) were the major components. Thirteen volatile oil compounds were identified in the E. citriodora leaf oil, of which citronellal (42.8%), citronellol (17.9%) and α-terpinene (11.2%) were the major components.

Mobility of 2-amino-4,6-dinitrobenzoic acid, a photodegradation product of TNT in a tropical soil under saturated abiotic conditions

We examined the mobility of 2-amino-4,6-dinitrobenzoic acid (2-A-4,6-DBA) a common photodegradation product of TNT, in soil taken from a former military training area on Oahu Island, Hawaii, USA. 2-A-4,6-DBA is stable and polar and has the potential to migrate to groundwater. Little experimentation has been conducted on explosives in tropical soils which differ chemically from soils in temperate climates. 2,4,6-Trinitrotoluene (TNT) and 1,3,5-hexahydro-1,3,5-trinitrotriazine (RDX) are the most commonly used secondary military explosives. Composition B (Comp B) is a frequently used 59/40/1 combination of RDX, TNT, and wax binder. In order to examine the effect of the presence of Comp B and its degradation products on the mobility of 2-A-4,6-DBA in soil, we dissolved field-collected Comp B fragments in water, exposed the solution to light and pumped it through soil and sand-packed stainless steel columns under abiotic saturated conditions. We found that in the presence of a complex mixture of explosives and degradation products, 2-A-4,6-DBA migrated faster than the parent compound (TNT) and other degradation products through both tropical soil and Ottawa sand (used as a reference) under sterile saturated conditions. The relatively rapid movement of 2-A-4,6-DBA suggests that it has the potential to contaminate underlying groundwater. However, the amount of 2-A-4,6-DBA produced under field conditions and its rate of biotic degradation were not part of this research, therefore, it is unknown how these factors might affect the transport and fate of 2-A-4,6-DBA.

Potential of Riverbank Filtration to Remove Explosive Chemicals

Riverbank filtration (RBF) is a low-cost and efficient water treatment technology for the removal of many surface water pollutants. It is widely used by water utilities in developed as well as developing countries to produce drinking water from surface water which is often polluted. In this research, the presence of explosive chemicals in riverbed sediments or in flowing water is considered as a potential threat to the quality of filtrate produced from RBF systems. For this, degradation experiments were conducted to examine the persistence of these compounds in river sediments. In addition, a model RBF system was setup to examine the breakthrough of the major explosive chemicals and their metabolites. Results show that HMX was the most mobile and compound followed by RDX. TNT and DNT degraded quickly. Thus, the presence of RDX and HMX could produce breakthroughs in high capacity collector wells located along riverbanks.