Access to Stereoblock Polyesters via Irreversible Chain-Transfer Ring-Opening Polymerization (ICT-ROP).

Precise control over polymer microstructure can enable the molecular tunability of material properties and represents a significant challenge in polymer chemistry. Stereoblock copolymers are some of the simplest stereosequenced polymers, yet the synthesis of stereoblock polyesters from prochiral or racemic monomers outside of "simple" isotactic stereoblocks remains limited. Herein, we report the development of irreversible chain-transfer ring-opening polymerization (ICT-ROP), which overcomes the fundamental limitations of single catalyst approaches by using transmetalation (e.g., alkoxide-chloride exchange) between two catalysts with distinct stereoselectivities as a means to embed temporally controlled multicatalysis in ROP. Our combined small-molecule model and catalytic polymerization studies lay out a clear molecular basis for ICT-ROP and are exploited to access the first examples of atactic-syndiotactic stereoblock (at-sb-st) polyesters, at-sb-st polyhydroxyalkanoates (PHAs). We achieve high levels of control over molecular weight, tacticity, monomer composition, and block structures in a temporally controlled manner and demonstrate that stereosequence control leads to polymer tensile properties that are independent of thermal properties.

Controlling pore structure and conductivity in graphene nanosheet films through partial thermal exfoliation.

Thermal exfoliation is an efficient and scalable method for the production of graphene nanosheets or nanoplatelets, which are typically re-assembled or blended to form new macroscopic "graphene-based materials". Thermal exfoliation can be applied to these macroscopic graphene-based materials after casting to create internal porosity, but this process variant has not been widely studied, and can easily lead to destruction of the physical form of the original cast body. Here we explore how the partial thermal exfoliation of graphene oxide (GO) multilayer nanosheet films can be used to control pore structure and electrical conductivity of planar, textured, and confined GO films. The GO films are shown to exfoliate explosively when the instrument-set heating rates are 100 K/min and above leading to complete destruction of the film geometry. Textured films with engineered micro-wrinkling and crumpling show similar thermal behavior to planar films. Here, we also demonstrate a novel method to produce fairly large size intact rGO films of high electrical conductivity and microporosity based on confinement. Sandwiching GO precursor films between inert plates during partial exfoliation at 250°C produces high conductivity and porosity material in the form of a flexible film that preserves the macroscopic structure of the original cast body.

Influence of External Heating Rate on the Structure and Porosity of Thermally Exfoliated Graphite Oxide.

Fast external heating rates in graphite oxide thermal exfoliation have been reported to be advantageous for generating high surface area graphene-based materials for a variety of applications. The study yields the surprising result that the surface area and porosity developed in reduced graphite oxide under some conditions are independent of instrument-set external heating rates. The true "total" heating rate experienced by the sample is shown to be the sum of the external rate and the local self-heating rate associated with the exothermicity of graphite oxide exfoliation, and under many conditions, the local self-heating contribution dominates. In these instances, increasing external heating rate does not increase the total rate, improve exfoliation degree or enhance surface area. These results are important for optimizing the conditions for fabrication of reduced graphene oxide with tailored properties.

Thermochemistry and kinetics of graphite oxide exothermic decomposition for safety in large-scale storage and processing.

The success of graphene technologies will require the development of safe and cost-effective nano-manufacturing methods. Special safety issues arise for manufacturing routes based on graphite oxide (GO) as an intermediate due to its energetic behavior. This article presents a detailed thermochemical and kinetic study of GO exothermic decomposition designed to identify the conditions and material compositions that avoid explosive events during storage and processing at large scale. It is shown that GO becomes more reactive for thermal decomposition when it is pretreated with OH- in suspension and the effect is reversible by back-titration to low pH. This OH- effect can lower the decomposition reaction exotherm onset temperature by up to 50 degrees of Celsius, causing overlap with common drying operations (100-120°C) and possible self-heating and thermal runaway during processing. Spectroscopic and modeling evidence suggest epoxide groups are primarily responsible for the energetic behavior, and epoxy ring opening/closing reactions are offered as an explanation for the reversible effects of pH on decomposition kinetics and enthalpies. A quantitative kinetic model is developed for GO thermal decomposition and used in a series of case studies to predict the storage conditions under which spontaneous self-heating, thermal runaway, and explosions can be avoided.

Explosive thermal reduction of graphene oxide-based materials: mechanism and safety implications.

Thermal reduction of graphene oxide or graphite oxide (GO) is an important processing step in the fabrication of many graphene-based materials and devices. Here we show that some bulk solid GO samples can undergo explosive decomposition when small samples are heated slowly in inert gas environments, while others do not. These micro-explosions can occur for samples as small as few milligrams and are sufficiently energetic to cause laboratory equipment damage. Thermochemical analysis methods are used to understand the factors that lead to the explosive reduction mode. The studies show that the explosive mode of reduction is caused by the exothermicity of GO reduction coupled with a threshold sample mass/size that causes heat and mass transfer limitations leading to local temperature rise and a thermal runaway reaction. The explosive mode of reduction is not caused or promoted by interstitial water, and its onset temperature can be lowered by immersion in potassium hydroxide solution. By allowing early release of internal gas pressure, the explosive mode reduces the extent of surface area development in GO exfoliation from an optimum value of 1470 m2g-1 obtained under non-explosive reduction conditions. Explosive reduction of bulk GO poses industrial safety hazards during large-scale storage, handling, and processing.

Porous Structures in Stacked, Crumpled and Pillared Graphene-Based 3D Materials.

Graphene, an atomically thin material with the theoretical surface area of 2600 m2g-1, has great potential in the fields of catalysis, separation, and gas storage if properly assembled into functional 3D materials at large scale. In ideal non-interacting ensembles of non-porous multilayer graphene plates, the surface area can be adequately estimated using the simple geometric law ~ 2600 m2g-1/N, where N is the number of graphene sheets per plate. Some processing operations, however, lead to secondary plate-plate stacking, folding, crumpling or pillaring, which give rise to more complex structures. Here we show that bulk samples of multilayer graphene plates stack in an irregular fashion that preserves the 2600/N surface area and creates regular slot-like pores with sizes that are multiples of the unit plate thickness. In contrast, graphene oxide deposits into films with massive area loss (2600 to 40 m2g-1) due to nearly perfect alignment and stacking during the drying process. Pillaring graphene oxide sheets by co-deposition of colloidal-phase particle-based spacers has the potential to partially restore the large monolayer surface. Surface areas as high as 1000 m2g-1 are demonstrated here through colloidal-phase deposition of graphene oxide with water-dispersible aryl-sulfonated ultrafine carbon black as a pillaring agent.

Adsorption of per- and polyfluoroalkyl substances on biochar derived from municipal sewage sludge.

Granular activated carbon (GAC) and ion exchange resin (IXR) are widely used as adsorbents to remove PFAS from drinking water sources and effluent waste streams. However, the high cost associated with GAC and IXR generation has motivated the development of less expensive adsorbents for treatment of PFAS-impacted water. Thus, the objective of this research was to create an economically viable and sustainable PFAS adsorbent from sewage sludge. Stepwise pyrolysis at temperatures from 300 °C to 1000 °C yielded biochars whose specific surface area (SSA) and porosity increased from 41 to 148 m2/g, and from 0.062 to 0.193 cm3/g, respectively. On a per organic char basis, the SSA of the biochar was as high as 1183 m2/g, which is comparable to commercially-available activated carbons. The adsorption of perfluorooctane sulfonic acid (PFOS) on sludge biochar increased with increasing pyrolysis temperature, which was positively correlated with increasing porosity and SSA. When 1000 °C processed biochar was tested with a mixture of eight PFAS, preferential adsorption of longer carbon chain-length species was observed, indicating the importance of PFAS hydrophobic interactions with the biochar and the availability of a wide range of mesopores. The adsorption of each PFAS was dependent upon both chain length and head group, with longer chain-length species exhibiting greater adsorption than shorter chain-length species, along with greater adsorption of species with sulfonic acid head groups compared to their chain length counterparts with carboxylic acid head groups. These findings demonstrate that biochar derived from municipal solid waste can serve as a cost-effective and sustainable adsorbent for the removal of PFOS and PFAS mixtures from source waters. The circular economy benefits and waste reduction potential associated with the use of sewage sludge-derived biochar supports the development of a viable sludge-derived biochar for the removal of PFAS from water.

Aerosol synthesis of cargo-filled graphene nanosacks.

Water microdroplets containing graphene oxide and a second solute are shown to spontaneously segregate into sack-cargo nanostructures upon drying. Analytical modeling and molecular dynamics suggest the sacks form when slow-diffusing graphene oxide preferentially accumulates and adsorbs at the receding air-water interface, followed by capillary collapse. Cargo-filled graphene nanosacks can be nanomanufactured by a simple, continuous, scalable process and are promising for many applications where nanoscale materials should be isolated from the environment or biological tissue.

Low-temperature persulfate activation by powdered activated carbon for simultaneous destruction of perfluorinated carboxylic acids and 1,4-dioxane.

Carbonaceous materials have emerged as a method of persulfate activation for remediation. In this study, persulfate activation using powdered activated carbon (PAC) was demonstrated at temperatures relevant to groundwater (5-25 °C). At room temperature, increasing doses of PAC (1-20 g L-1) led to increased persulfate activation (3.06 × 10-6s-1 to 2.10 × 10-4 with 1 and 20 g L-1 PAC). Activation slowed at lower temperatures (5 and 11 °C); however, substantial (>70 %) persulfate activation was achieved. PAC characterization showed that persulfate is activated at the surface of the PAC, as indicated by an increase in the PAC C:O ratio. Similarly, electron paramagnetic resonance (EPR) spectroscopy studies with a spin trapping agents (5,5-dimethyl-1-pyrroline N-oxide (DMPO)) and 2,2,6,6-tetramethylpiperidine (TEMP) revealed that singlet oxygen was not the main oxidizing species in the reaction. DMPO was oxidized to form 5,5-dimethylpyrrolidone-2(2)-oxyl-(1) (DMPOX), which forms in the presence of strong oxidizers, such as sulfate radicals. The persulfate/PAC system is demonstrated to simultaneously degrade both perfluorooctanoic acid (PFOA) and 1,4-dioxane at room temperature and 11 °C. With a 20 g L-1 PAC and 75 mM persulfate, 80 % and 70 % of the PFOA and 1,4-dioxane, respectively, degraded within 6 h at room temperature. At 11 °C, the same PAC and persulfate doses led to 57% dioxane degradation and 54 % PFOA degradation within 6 h. Coupling PAC with persulfate offers an effective, low-cost treatment for simultaneous destruction of 1,4-dioxane and PFOA.

Antioxidant deactivation on graphenic nanocarbon surfaces.

This article reports a direct chemical pathway for antioxidant deactivation on the surfaces of carbon nanomaterials. In the absence of cells, carbon nanotubes are shown to deplete the key physiological antioxidant glutathione (GSH) in a reaction involving dissolved dioxygen that yields the oxidized dimer, GSSG, as the primary product. In both chemical and electrochemical experiments, oxygen is only consumed at a significant steady-state rate in the presence of both nanotubes and GSH. GSH deactivation occurs for single- and multi-walled nanotubes, graphene oxide, nanohorns, and carbon black at varying rates that are characteristic of the material. The GSH depletion rates can be partially unified by surface area normalization, are accelerated by nitrogen doping, and suppressed by defect annealing or addition of proteins or surfactants. It is proposed that dioxygen reacts with active sites on graphenic carbon surfaces to produce surface-bound oxygen intermediates that react heterogeneously with glutathione to restore the carbon surface and complete a catalytic cycle. The direct catalytic reaction between nanomaterial surfaces and antioxidants may contribute to oxidative stress pathways in nanotoxicity, and the dependence on surface area and structural defects suggest strategies for safe material design.

Libraries of Uniform Magnetic Multicore Nanoparticles with Tunable Dimensions for Biomedical and Photonic Applications.

Multicore iron oxide nanoparticles, also known as colloidal nanocrystal clusters, are magnetic materials with diverse applications in biomedicine and photonics. Here, we examine how both of their characteristic dimensional features, the primary particle and sub-micron colloid diameters, influence their magnetic properties and performance in two different applications. The characterization of these basic size-dependent properties is enabled by a synthetic strategy that provides independent control over both the primary nanocrystal and cluster dimensions. Over a wide range of conditions, electron microscopy and X-ray diffraction reveal that the oriented attachment of smaller nanocrystals results in their crystallographic alignment throughout the entire superstructure. We apply a sulfonated polymer with high charge density to prevent cluster aggregation and conjugate molecular dyes to particle surfaces so as to visualize their collection using handheld magnets. These libraries of colloidal clusters, indexed both by primary nanocrystal dimension (dp) and overall cluster diameter (Dc), form magnetic photonic crystals with relatively weak size-dependent properties. In contrast, their performance as MRI T2 contrast agents is highly sensitive to cluster diameter, not primary particle size, and is optimized for materials of 50 nm diameter (r2 = 364 mM-1 s-1). These results exemplify the relevance of dimensional control in developing applications for these versatile materials.

High capacity mercury adsorption on freshly ozone-treated carbon surfaces.

A set of carbon materials was treated by a choice of common oxidizers to investigate the mercury capture capacities at varying temperature conditions. It was found that ozone treatment dramatically increases the mercury capture capacity of carbon surfaces by factors up to 134, but the activity is easily destroyed by exposure to the atmosphere, to water vapor, or by mild heating. Freshly ozone-treated carbon surfaces are shown to oxidize iodide to iodine in solution and this ability fades with aging. FTIR analysis shows broad C-O stretch features from 950 to 1300 cm(-1), which decay upon atmospheric exposure and are similar to the C-O-C asymmetric stretch features of ethylene secondary ozonide. The combined results suggest that the ultra-high mercury capture efficiency is due to a subset of labile C-O functional groups with residual oxidizing power that are likely epoxides or (epoxide-containing) secondary ozonides. The results open the possibility for in situ ozonolysis to create high-performance carbon-based Hg sorbents.

Counting calories in Drosophila diet restriction.

The extension of life span by diet restriction in Drosophila has been argued to occur without limiting calories. Here we directly measure the calories assimilated by flies when maintained on full- and restricted-diets. We find that caloric intake is reduced on all diets that extend life span. Flies on low-yeast diet are long-lived and consume about half the calories of flies on high-yeast diets, regardless of the energetic content of the diet itself. Since caloric intake correlates with yeast concentration and thus with the intake of every metabolite in this dietary component, it is premature to conclude for Drosophila that calories do not explain extension of life span.

Template synthesis of nanophase mesocarbon.

Templating techniques are used increasingly to create carbon materials with precisely engineered pore systems. This article presents a new templating technique that achieves simultaneous control of pore structure and molecular (crystal) structure in a single synthesis step. With the use of discotic liquid crystalline precursors, unique carbon structures can be engineered by selecting the size and geometry of the confining spaces and selecting the template material to induce edge-on or face-on orientation of the discotic precursor. Here mesophase pitch is infiltrated by capillary forces into a nanoporous glass followed by slow carbonization and NaOH etching. The resulting porous carbon material exhibits interconnected solid grains about 100 nm in size, a monodisperse pore size of 60 nm, 42% total porosity, and an abundance of edge-plane inner surfaces that reflect the favored edge-on anchoring of the mesophase precursor on glass. This new carbon form is potentially interesting for a number of important applications in which uniform large pores, active-site-rich surfaces, and easy access to interlayer spaces in nanometric grains are advantageous.

Antioxidant chemistry of graphene-based materials and its role in oxidation protection technology.

Two-dimensional nanomaterials have potential as a new class of antioxidants that combine physical barrier function with ultrahigh surface area for free radical scavenging. This work presents the first measurements of the chemical reactivities of graphene-based materials toward a set of model free radicals and reactive oxygen species using electron paramagnetic resonance spectroscopy (EPR) and sacrificial dye protection assays. Graphene-based materials are shown to protect a variety of molecular targets from oxidation by these species, and to be highly effective as hydroxyl-radical scavengers. When the hydroxyl radical is produced photolytically, the overall antioxidant effect is a combination of preventative antioxidant activity (UV absorption) and ˙OH radical scavenging. Few-layer graphene is more active than monolayer graphene oxide, despite its lower surface area, which indicates that the primary scavenging sites are associated with the sp(2)-carbon network rather than oxygen-containing functional groups. To explain this trend, we propose that GO is a weak hydrogen donor, due to the non-phenolic nature of most OH groups on GO, which reside at basal sp(3)-carbon sites that do not allow for radical resonance stabilization following hydrogen donation. As an example application of graphene antioxidant behavior, we show that encapsulation of TiO2 nanoparticles in graphene nanosacks reduces undesired photo-oxidative damage to nearby organic target molecules, which suggests graphene encapsulation as a new approach to managing adverse environmental or health impacts of redox-active nanomaterials.

Encapsulation of particle ensembles in graphene nanosacks as a new route to multifunctional materials.

Hybrid nanoparticles with multiple functions are of great interest in biomedical diagnostics, therapies, and theranostics but typically require complex multistep chemical synthesis. Here we demonstrate a general physical method to create multifunctional hybrid materials through aerosol-phase graphene encapsulation of ensembles of simple unifunctional nanoparticles. We first develop a general theory of the aerosol encapsulation process based on colloidal interactions within drying microdroplets. We demonstrate that a wide range of cargo particle types can be encapsulated, and that high pH is a favorable operating regime that promotes colloidal stability and limits nanoparticle dissolution. The cargo-filled graphene nanosacks are then shown to be open structures that rapidly release soluble salt cargoes when reintroduced into water, but can be partially sealed by addition of a polymeric filler to achieve slow release profiles of interest in controlled release or theranostic applications. Finally, we demonstrate an example of multifunctional material by fabricating graphene/Au/Fe3O4 hybrids that are magnetically responsive and show excellent contrast enhancement as multimodal bioimaging probes in both magnetic resonance imaging and X-ray computed tomography in full-scale clinical instruments.

Mercury vapor release from broken compact fluorescent lamps and in situ capture by new nanomaterial sorbents.

The projected increase in the use of compact fluorescent lamps (CFLs) motivates the development of methods to manage consumer exposure to mercury and its environmental release at the end of lamp life. This work characterizes the time-resolved release of mercury vapor from broken CFLs and from underlying substrates after removal of glass fragments to simulate cleanup. In new lamps, mercury vapor is released gradually in amounts that reach 1.3 mg or 30% of the total lamp inventory after four days. Similar time profiles but smaller amounts are released from spent lamps or from underlying substrates. Nanoscale formulations of S, Se, Cu, Ni, Zn, Ag, and WS2 are evaluated for capture of Hg vapor under these conditions and compared to conventional microscale formulations. Adsorption capacities range over 7 orders of magnitude, from 0.005 (Zn micropowder) to 188 000 microg/g (unstabilized nano-Se), depending on sorbent chemistry and particle size. Nanosynthesis offers clear advantages for most sorbent chemistries. Unstabilized nano-selenium in two forms (dry powder and impregnated cloth) was successfully used in a proof-of-principle test for the in situ, real-time suppression of Hg vapor escape following CFL fracture.