Renewable Resources and Enzymatic Processes to Create Functional Polymers: Adapting Materials and Reactions from Food Processing

We are exploiting materials and concepts from food science to create functionalized, environmentally friendly derivatives of the biopolymer chitosan, a byproduct of seafood processing. Functional groups are grafted onto chitosan using tyrosinase, the enzyme responsible for food browning. The functionalizing groups studied include low-molecular-weight phenols derived from natural sources and high-molecular-weight proteins. The approach of using low-molecular-weight phenols to functionalize chitosan is illustrated with arbutin, a natural phenol found in pears. Results demonstrate that tyrosinase initiates reactions that lead to the conversion of arbutin–chitosan solutions into gels. These gels can be rapidly broken by treatment with the chitosan-hydrolyzing enzyme chitosanase, demonstrating that the chitosan derivatives remain biodegradable. We briefly review other studies in which low-molecular-weight natural phenols are enzymatically grafted onto chitosan to confer functional properties. The creation of co-polymers is illustrated by results in which tyrosinase is used to couple gelatin onto chitosan. Gelatin is a proteinaceous byproduct of meat production. The tyrosinase-generated gelatin–chitosan conjugates have been observed to offer interesting rheological and thermal properties. These results demonstrate the potential for using renewable resources and enzymatic processing to create environmentally friendly polymers with useful functional properties.     

Phosphorus recovery from secondary effluent and side-stream liquid in a sewage treatment plant using zirconium-loaded saponified orange waste

Zirconium was loaded onto orange waste, a cheap and available agricultural waste in Japan, to investigate the feasibility of its utilization for phosphorus recovery from secondary effluent and side-stream liquid, which contain 5.9 and 68.2 mg/dm³ phosphorus, respectively. The phosphorus removal from side-stream liquid by using zirconium-loaded saponified orange waste (Zr-SOW) gel increased with an increasing solid/liquid ratio, and it was found that Zr-SOW gel showed better performance than zirconium ferrite. The prepared adsorbent was effective for phosphorus removal and exhibited a reasonably high adsorption capacity, twice than that of zirconium ferrite. The secondary effluent was treated in a column packed with Zr-SOW gel, and an dynamic adsorption capacity of 1.3 mol-P/kg was attained. The adsorbed phosphorus from the column was successfully eluted as a concentrated form by using a small amount of 0.2 M NaOH. Throughout the elution process, zirconium was not leaked from the adsorption gel.     

Poly(Ethylene Glycol) Grafted Starch Introducing a Novel Interphase in Poly(Lactic Acid)/Poly(Ethylene Glycol)/Starch Ternary Composites

The main purpose of this study is challenging to dramatically improve the toughness of poly(lactic acid) (PLA)/starch by adding poly (ethylene glycol) (PEG) into the composites and grafting PEG molecules onto the surface of starch particles. It was found that the surface grafting of PEG onto starch induced the presence of PEG-rich regions located around the starch particles, caused by migration and aggregation of free PEG molecules. A novel interphase transition layer between PLA and starch was formed, which showed great ability for cavitation and vested large-scaled plastic deformation to PLA matrix. Further mechanical properties tests indicated the formation of interphase layer significantly increase the elongation at break from 10.2 to 254.5%, and notched impact strength from 1.56 to 2.37?kJ/m² for PLA/PEG/starch ternary composites. The influence of PEG component, ethanol extraction and annealing was also investigated.     

Biosorptive removal of Pb(II) and Cu(II) from wastewater using activated carbon from cassava peels

The ability of activated carbon from cassava peels to remove heavy metals like Cu(II) and Pb(II) from hospital wastewater was investigated. The study showed that a pH of 8 was the best for the sorption of both metal ions onto the biosorbent. The time-dependent experiments for the metal ions showed that the binding of the metal ions to the biomass was rapid and occurred within 20–120 min. Sorption efficiency increased with a rise in adsorbent dosage. It increased from 12 to 73 % for Pb(II) and 26 to 79 % for Cu(II) when the adsorbent dose increased from 2 to 12 g. An increase in temperature led to an increase in sorption for both metal ions. The Langmuir model showed that the biomass has a higher sorption capacity for Cu(II) than Pb(II), with q _m = 5.80 mg g^?1 for Pb(II) and 8.00 mg g^?1 for Cu(II). The Freundlich isotherm K _f was 1.4 for Pb(II) and 1.8 for Cu(II), indicating a preferential sorption of Cu(II) onto the biosorbent. Adsorption capacity was found to decrease with an increase in particle sizes. Sorption occurred by physical mechanisms and was mainly controlled by intraparticle diffusion.     

Remediation of a Diffuse Trichloroethene Plume in an Urban Setting

During an environmental assessment of a former fleet vehicle maintenance facility located in Jacksonville, Florida, dissolved trichloroethene (TCE) concentrations exceeding the Florida groundwater standard (3 micrograms per liter) were detected at a depth of 40 feet (12 meters) below land surface (bls). A plume was delineated that measured approximately 600 feet (183 meters) by 150 feet (46 meters), extending across a major road and onto adjacent properties. Shaw Environmental, Inc., which was acquired by CB&I in February 2012, performed pilot tests with in situ oxygen curtain (iSOC), and the injection of Anaerobic Biochem Plus (ABC+), a mixture of lactates, a phosphate buffer, fatty acids, and zero‐valent iron. Based on the pilot‐test results, ABC+ appeared the more effective of the two methods and was selected for full‐scale implementation. In February 2011, Shaw Environmental, Inc. and a subcontractor used direct‐push technology to inject ABC+ in 120 borings. By September 2011, the treatment succeeded in lowering the concentrations of TCE to below the Florida standard in all impacted wells. Subsequent sampling events indicate that TCE concentrations have remained below the standard, but sampling continues for iron, which is decreasing but remains slightly elevated. © 2013 Wiley Periodicals, Inc.     

Status and prospects of pay-as-you-throw in Europe - a review of pilot research and implementation studies

Over the past 20 years, significant advances have been made in developing efficient schemes to charge households for their actual waste generation. Viable fee models and technical solutions which are applicable to different environments and provide waste generators with individual incentives for waste diversion efforts have increased the recognition of pay-as-you-throw (PAYT) as an effective instrument for recycling-oriented waste management and financing. On this basis, PAYT has become a practical reality in an increasing number of countries in Europe. Even countries with traditional reservations for direct charging have started to make consideration of PAYT in the revision of their national policy programmes. A situational analysis performed at the European level showed that detailed insights regarding the concrete reactions, red flags and wider benefits inherent to such scheme may still have to be further dispersed in order to overcome the caveats on PAYT and eventually adopt the approach on a larger scale. Claims that the results of PAYT applications are only local in meaning can be disproved as many of the developments bear universal character and can be verified even for larger territories using such schemes in different ways. Including results from an international research co-operation and comparative studies conducted in Germany, this article examines the state-of-the-art of PAYT and shades light onto some of the generally observed implications of its implementation. In conclusion, an outlook on the further potentials and propagation of this scheme is given.     

Adsorptive Removal of Malachite Green Chloride and Reactive Red-198 from Aqueous Solutions by Using Multiwall Carbon Nanotubes-Graft-Poly (2-acrylamido-2-methyl-1-propanesulfonic acid)

The multiwall carbon nanotubes (MWCNTs) were modified by 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) via grafting reaction and γ-rays of ⁶⁰Co source was used as initiator. The outcome product was called hydroxyethylated (HOEt-MWCNTs) graft poly(AMPS) and abbreviated as HOEt-MWCNTs-g-PAMPS. The parameters that affected the grafting yield were optimized. The maximum grafting obtained was ~20 %. HOEt-MWCNTs-g-PAMPS were characterized by Fourier transform infra red, scanning electron microscopy, high resolution transmission electron microscopy, thermal gravimetric analysis. The adsorptive removals of malachite green chloride (MGC) and reactive red 198 (RR-198) onto HOEt-MWCNTs-g-PAMPS were studied at variable conditions. The adsorption isotherms were analyzed using Langmuir, Redlich–Peterson, Freundlich, Khan and Sips models. The results referred that Sips model is the best fitting to adsorption of MGC and Freundlich model is the best fitting to RR-198 adsorption. The monolayer coverage capacities of HOEt-MWCNTs-g-PAMPS for MGC and RR-198 dyes were found 172 and 323 mg g^?1, respectively. The rate of kinetic adsorption processes of MGC and RR-198 onto HOEt-MWCNTs-g-PAMPS were described by using pseudo-first order, pseudo-second order and intraparticle diffusion models. The pseudo-first order and pseudo-second order models were the best choice among the kinetic models to depict the adsorption behaviors of MGC and RR-198 dyes onto HOEt-MWCNTs-g-PAMPS, respectively. Further, the effect of temperature on the adsorption isotherms was investigated and the thermodynamic parameters were obtained. The results indicated that the adsorption process is spontaneous and endothermic. The values of ΔG° varied in range with the mean values showing a gradual increase from ?3.17 to ?3.64 kJ mol^?1 for MGC and ?3.36 to ?3.73 kJ mol^?1 for RR-198. The reusability and regeneration of adsorbent were investigated. The outcome data referred to that the efficiency of adsorbent >98 %. The outline results declared that there is a good potentiality for the HOEt-MWCNTs-g-PAMPS to be used as an adsorbent for the removal of MGC and RR-198 from aqueous solutions.     

Papermill industrial waste as a sustainable source for high efficiency absorbent production

Papermill sludge (PMS) is generated during the wastewater treatment process of paper production. Its handling and disposal techniques are of great concern for the environment. It can be landfilled as a waste, or it can be recycled and converted into useful products of high value. It has a very promising application as an absorbing agent for the cleaning of water surfaces polluted with hydrophobic substances (vegetable, synthetic and mineral oils, animal fats, fuels, organic chemicals and even coal dust). Here, we present the pretreatment procedure (hydrophobation, mechanical and thermal treatments) of PMS that produces a lightweight absorbent material (HAWSC - high efficiency absorbent for water surface cleaning), which floats on the water surface and binds hydrophobic pollutants with considerably higher efficiency than commercially available mineral and synthetic absorbents. After its application, it can be incinerated, due to its high caloric value, to produce energy. The incineration residues can then be formed into granules that can be used as an efficient absorbent for fluids spilled onto solid surfaces.     

Role of Hydrophilic and Hydrophobic Interactions in Structure Development of Zein Films

Zein has been studied for its potential as a biobased polymeric material. Due to the fact that films made exclusively from zein are brittle, composites of zein and oleic acid were prepared in our lab and formed into flexible films. Film properties were believed related to their structure. X-ray scattering measurements on zein films suggested the formation of layers along the plane of the film. Oleic acid seemed to play an important role in layer formation. However, X-ray measurements could not yield information on the nature of the interface between oleic acid and zein. Surface plasmon resonance (SPR) was used to further investigate interaction between zein and oleic acid. Dynamic adsorption of zein from alcoholic solutions onto hydrophilic and hydrophobic surfaces generated by self-assembled monolayers of 11-mercaptoundecanoic acid or 1-octanethiol was monitored by SPR. It was observed that zein had a greater affinity for hydrophilic than for hydrophobic surfaces under the prevalent experimental conditions. A mechanism for structure development of zein-oleate films was proposed based on these results and previous X-ray measurements. It is suggested that the structure development involves hydrophilic adsorption of fatty acids onto the zein surface followed by hydrophobic associations leading to a layered film structure organization.     

Distributed inner states TiO2-coated plastic fibers as photocatalysts for decomposing organic pollutants in water

A new method for decomposing organic pollutants in water is proposed. First, we used less pure titanium dioxide (TiO₂) particles as a photocatalyst material to achieve an absorption band that would be as wide as the spectrum for visible sunlight. The TiO₂ particles were coated onto the surface of transparent plastic fibers and used to decompose test solutions of rhodamine that were placed in open sunlight for several days. We observed an effective decomposition, and after completing the decomposition process, the fibers could be removed easily from the cleaned water leaving no TiO₂ in the water. Because there was no significant change in the elemental composition of the fiber surface after being used for cleaning the water, the coated fiber can be used repeatedly.     

Measuring Aerosol and Heavy Metal Deposition on Urban Woodland and Grass Using Inventories of 210Pb and Metal Concentrations in Soil

The deposition of aerosols to trees has proved very difficult to quantify, especially in complex landscapes. However, trees are widely quoted to be efficient scavengers of particles from the atmosphere, and a growing proportion of the pollutant burden in the atmosphere is present in the aerosol phase. In this study, the deposition of aerosols onto woodland and grass was quantified at a range of locations throughout the West Midlands of England. The sites included mature deciduous woodland in Edgbaston, and Moseley, and mixed woodland at sites within Sutton Park, a large area of semi-natural vegetation. Aerosol deposition to areas of grassland close to the woodland at each site was also measured. Detailed inventories of ²¹⁰Pb in soils within the woodland and in grassland soils, together with concentrations in the atmosphere and precipitation, provided the necessary data to calculate the long-term (about 40 years) annual deposition of sub-micron aerosols onto grassland and woodland. The soil inventories of ²¹⁰Pb under woodland exceeded those under grass, by between 22% and 60%, with dry deposition contributing 24% of the total input flux for grass and 47% for woodland. The aerosol dry deposition velocity to grassland averaged 3.3 mm s^-1 and 9 mm s^-1 for woodland. The large deposition rates of aerosols onto woodland relative to grass or other short vegetation (× 3), and accumulation of heavy metals within the surface horizons of organic soils, leads to large concentrations in soils of urban woodland. Concentrations in the top 10 cm of these woodland soils averaged 252 mg kg^-1 for Pb with peaks to 400 mg kg^-1. Concentrations of Cd averaged 1.4 mg kg^-1, Cu, 126 mg kg^-1, Ni 23 mg kg^-1 and Zn 173 mg kg^-1. The accumulated Pb in urban woodland soils is shown to be large relative to UK emissions.     

有机硅改性泥炭的吸附性能研究

采用三甲基氯硅烷处理泥炭(泥炭硅烷化),使其吸附性能得以改善。采用硅烷化泥炭自水溶液中吸附苯甲酸、苯甲醛和苯酚的等温线进行测定,对吸附过程的△G、△H和△s进行计算。试验结果表明：熵变是这类体系吸附过程的重要驱动力;硅烷化后的泥炭表面的疏水性明显增强,对水溶液中芳香族化合物的吸附量增大。     

Treatment of a high-strength sulphate-rich alkaline leachate using an anaerobic filter

The research looks at the feasibility of treating an alkaline sulphate-rich leachate arising from the co-disposal of municipal solid waste with cement kiln dust by means of an anaerobic filter (AF). This type of leachate with a high sulphate concentration is commonly prohibited for discharge to sewer and requires an on-site treatment solution. The AF used had a working volume of 4l and contained reticulated polyurethane foam as the biomass support material. The filters were operated over a 152 day experimental period during which the COD loading onto the filter was increased from 0.76 to 7.63kgCODm(-3)d(-1). In the early stages of operation at low loading, soluble sulphides accumulated that inhibited methanogenic activity. This was restored by dosing FeCl(3) to the reactor. The continued dosing allowed efficient COD removal of between 75% and 90% until the nominal retention time in the reactor was 3 days, at which point reactor performance declined significantly. The main mechanism for COD removal was by sulphate-reducing bacteria, which also resulted in up to 88% sulphate removal from the leachate. The average methane generation rate was 0.10lg(-1) COD removed. The results indicate the potential for using this approach as a pre-treatment that could significantly reduce the COD load to a second stage treatment process, but problems associated with the implementation of the technology at a larger scale have been identified.     

Transformation of Particle-Bound Phosphorus at the Land–Sea Interface in a Danish Estuary

Danish rivers carry >50% of the phosphorus (P) transport as particulate P (PP). In five of six rivers sampled in November 1998 iron-bound P made up > 59% of PP and loosely adsorbed P ranged between 2% and 13%. This fraction could potentially be released in 14‰ seawater. The behaviour of dissolved and particulate P fractions was studied during seven month in a 2 km long estuary with low freshwater retention time and low tidal range. The river carried ∼10% of PP as loosely adsorbed P but increased concentrations of dissolved inorganic P (DIP) relative to the estuarine mixing line was only observed in the summer month with low freshwater flow and was more likely due to DIP release from the bottom sediment. Instead estuarine particles were always enriched with oxidized iron (ox.Fe) and iron-bound P as well as loosely adsorbed P and during May–September this coincided with increasing concentration of PP in estuary. We suggest that flocculation of ox.Fe and adsorption of DIP onto the particles with subsequent transport seawards is a major loss process for P during the summer month. During winter month where 85% of the run-off occurs the dominant process in the estuary is sedimentation of larger particles, however, a comparison of river particles with surface sediment clearly reveals that most PP is mobilized again from the bottom sediments.     

Agricultural waste biomass converted to activated carbon as a material for gold processing

Waste biomass in the form of coconut shells was pyrolyzed and activated with steam to produce activated carbons, which were then assessed for their potential for use in the processing of gold. Activated carbons with different amounts of carbon burn-off were prepared by steam activation of carbonized coconut shells. Carbonization of the shells was performed at a pyrolysis temperature of 600?°C and the resulting chars were activated in steam at a gasification temperature of 900?°C and various durations of activation time. Textural characteristics of the derived activated carbons were determined and their effects on gold adsorption from an acidified gold chloride solution were studied. The surface area and porosity of the activated carbons increased with activation time up to 59 wt?% carbon burn-off. A further increase in the burn-off resulted in the loss of structural walls between pores and consequently, a decline in the surface area and porosity of the activated carbons. The gold adsorption capacity and rate of gold adsorption from the gold chloride solution onto the activated carbons were found to increase significantly with the total pore and micropore volumes of the activated carbons.     

Synthesis and Characterization of Biodegradable Starch-Polyacrylamide Graft Copolymers Using Starches with Different Microstructures

The effects of starch structures, in particular amylose content, on grafting reactions were investigated using thermal gravimetric analysis (TGA), nuclear magnetic resonance, X-ray diffraction (XRD). As a model system, corn starches with different amylose contents (0, 26, 50 and 80 %) were grafted onto acrylamide to produce superabsorbent polymers (SAPs). The weight loss measured by TGA at different temperature was used to analyze the grafting ratio in quantity. In general, the grafting ratio increased (about 10 %) with increasing starch amylose content, and graft chain segment lengths were much lower for the amylopectin-rich (waxy) starch. The high molecular weight and branched structure of the amylopectin reduced the mobility of the polymer chains and increased viscosity, which resulted in resistance to chain growth. The water absorption capability was increased with increasing amylose content for the starch-based SAPs. XRD detection showed that the crystalline structure of all starches was destroyed after grafting reactions. The thermal stability of the polyacrylamide grafted onto the starches increased by about 10 °C, which could be explained by the strong bonding between the grafted polymer chains and the starch matrices.     

Removal of substituted phenols onto iron‐treated Nostoc sp. biomass

This study explored the possibility of removing 4‐nitrophenol (4‐NP) and 2,4‐dichlorophenol (2,4‐DCP) from water by using a dead blue‐green algae, Nostoc sp., dried and untreated and dried and treated with iron (Fe‐treated with 0.1 M ferric chloride solution for 1 day). The Nostoc sp. untreated and Fe‐treated biomass were used to study the sorption and desorption of 4‐NP and 2,4‐DCP. The effects of solute concentration, ionic strength, and temperature on sorption and desorption in the presence of untreated and treated Nostoc sp. biomass were investigated. The Fe‐treated Nostoc sp. biomass sorbed higher amounts of both 4‐NP and 2,4‐DCP than the untreated biomass. The percent cumulative desorption decreased from 6.41% to 0.28% and 1.84% to 0.19%, respectively, for 4‐NP and 2,4‐DCP for the Fe‐treated biomass. Biosorption of 4‐NP and 2,4‐DCP onto untreated and Fe‐treated Nostoc sp. biomass conformed to Freundlich isotherms. Iron treatment of Nostoc sp. biomass increased the value of ln K from 8.07 to 8.59 for 4‐NP and from 8.04 to 8.51 for 2,4‐DCP but decreased their desorption. An increase in ionic strength (0.003–0.03) increased the biosorption of both substituted phenols and decreased their percent desorption. An increase in temperature in the range of 15–35°C decreased the sorption of 4‐NP and 2,4‐DCP onto both untreated and Fe‐treated Nostoc sp. biomass and increased their desorption, indicating that the biosorption of both substituted phenols onto untreated and Fe‐treated Nostoc sp. biomass was principally a physical process. The results of this study suggest that Fe‐treated dried Nostoc sp. biomass could be explored as an inexpensive and eco‐friendly material for the effective removal of these phenols and, potentially, other chemicals from industrial wastewater and contaminated groundwater.     

Augmenting in-situ remediation by soil vapor extraction with six-phase soil heating

The use and performance of soil vapor extraction (SVE) as an in-situ remedial technology has been limited at numerous sites because of both geologic and chemical factors. SVE systems are not well suited to sites containing low permeability soils or sites contaminated with recalcitrant compounds. Six-phase soil heating (SPSH) has been developed by the Battelle Pacific Northwest Laboratories (Battelle) to enhance SVE systems. The technology utilizes resistive soil heating to increase the vapor pressure of subsurface contaminants and to generate an in-situ source of steam. The steam strips contaminants sorbed onto soil surfaces and acts as a carrier gas, providing an enhanced mechanism by which the contaminants can reach an extraction well. Full-scale applications of SPSH have been performed at the U.S. Department of Energy's Savannah River Site in Aiken, South Carolina; at a former fire training site in Niagara Falls, New York; and at Fort Richardson near Anchorage, Alaska. At each site, chlorinated solvents were present in low permeability soils and SPSH was applied in conjunction with SVE. The results of the three applications showed that SPSH is a cost-effective technology that can reduce the time required to remediate a site using only conventional SVE.     

Neutralization of an extremely acidic sludge and stabilization of heavy metals in flyash aggregates

An extremely acidic, heavy metal-rich sludge (pH=-1.2) was scrubbed with a Class-F fly ash in order to simultaneously neutralize the acidity and stabilize the heavy metals contained in both wastes. This paper outlines the leaching behavior of the aggregate material generated by scrubbing. For proper fly ash/sludge ratios, the fly ash acted as an outstanding neutralizer for the acidic waste. Leaching of heavy metals from the aggregate samples was below the environmental limits within a pH range between 3 and 9. Subsequent washing of the leached aggregate with acidic CALWET solutions did not result in an additional release of heavy metals. It is proposed that coordinative bonding of the metal cations onto neutral surface sites and electrostatic adsorption led to stabilization of the heavy metals within the aggregate structure below hydrolysis pHs.     

Thorium(IV) Recovery from Water and Sea Water Using Surface Modified Nanocellulose/Nanobentonite Composite: Process Design

Thorium(Th) contamination in the ground water an emerging environmental issue and Th recovery from sea water and nuclear wastewater is of high significance, as it is a major player in the energy sector. For the adsorption and recovery of Th, polymer grafted bio materials are reported as most efficient materials. P(IA/MAA)-g-NC/NB was prepared and all the steps in the synthetic routes were monitored using FTIR, SEM–EDS, and XRD, TG. Efficiency in removal of Th(IV) by P(IA/MAA)-g-NC/NB was tested by batch adsorption technique. The pH dependent Th(IV) adsorption process, was optimized at 4.5 and adsorption equilibrium was achieved within 120 min. Experimental kinetic data correlates well with pseudo-second-order equation, indicates adsorption was chemical process via ion exchange followed by complexation reaction, also could explain the film diffusion process of adsorption. Sips isotherm proved to best fit for the adsorption of Th(IV) onto P(IA/MAA)-g-NC/NB with maximum adsorption capacity of 95.19 mg/g. Thermodynamic studies revealed the endothermic nature, feasibility and spontaneity of the adsorption process. ΔHx and ΔSx were decreased to a small extent from ?5.567 to ?3.439 kJ/mol and increased from 11.18 to 18.39 J/mol, respectively, with increase in surface loading from 50 to 70 mg/g, indicating that the surface of the onto P(IA/MAA)-g-NC/NB is having energetically heterogeneous surface and there may be some lateral interactions between the adsorbed Th(IV) ions Repeated adsorption–desorption study over six cycles, adsorption percentage decreases from 99.0 to 94.6 %, proved the efficiency of P(IA/MAA)-g-NC/NB as an effective adsorbent for the removal and recovery of Th(IV) from aqueous solutions. Complete removal of Th(IV) ions from seawater containing 10 mg/L with a dose of 0.25 g/L P(IA/MAA)-g-NC/NB achieved. Batch adsorption system as double stage reactor designed from the adsorption isotherm data of Th(IV) by constructing operational lines. From these could be concluded that P(IA/MAA)-g-NC/NB is a promising candidate for the effective removal and removal of Th(IV) from industrial effluents phase and sea water. The maximum adsorption capacity Qs for Ceralite IRC-50 calculated which was found to be 179.67 mg/g which are considerably lower than those for P(IA/MAA)-g-NC/NB.