Joseph M. Azzarelli

Rapid prototyping of carbon-based chemiresistive gas sensors on paper

Significance This paper describes a rapid, solvent-free, two-step procedure for the fabrication of selective gas and vapor sensors from carbon nanotubes and graphite on the surface of paper that overcomes challenges associated with solvent-assisted chemical functionalization and integration of these materials into devices. The first step generates solid composites from carbon nanotubes (or graphite) and small molecules (chosen to interact with specific types of gases and vapors) by mechanical mixing and subsequent compression into a form similar to a conventional pencil “lead”. The second step uses mechanical abrasion (“drawing”) of these solid composites on the surface of paper to generate functional devices. The use of diverse composites yields sensing arrays capable of detecting and differentiating gases and vapors and part-per-million concentrations. Chemically functionalized carbon nanotubes (CNTs) are promising materials for sensing of gases and volatile organic compounds. However, the poor solubility of carbon nanotubes hinders their chemical functionalization and the subsequent integration of these materials into devices. This manuscript describes a solvent-free procedure for rapid prototyping of selective chemiresistors from CNTs and graphite on the surface of paper. This procedure enables fabrication of functional gas sensors from commercially available starting materials in less than 15 min. The first step of this procedure involves the generation of solid composites of CNTs or graphite with small molecule selectors—designed to interact with specific classes of gaseous analytes—by solvent-free mechanical mixing in a ball mill and subsequent compression. The second step involves deposition of chemiresistive sensors by mechanical abrasion of these solid composites onto the surface of paper. Parallel fabrication of multiple chemiresistors from diverse composites rapidly generates cross-reactive arrays capable of sensing and differentiating gases and volatile organic compounds at part-per-million and part-per-thousand concentrations.

An Atom-Economic Synthesis of Nitrogen Heterocycles from Alkynes

A robust route to 2,4-disubstituted pyrrole heterocycles relying upon a cascade reaction is reported. The reaction benefits from operational simplicity: it is air and moisture tolerant and is performed at ambient temperature. Control over the reaction conditions provides ready access to isopyrroles, 2,3,4-trisubstituted pyrroles, and 3-substituted pyrollidin-2-ones.

Wireless gas detection with a smartphone via rf communication

Significance This paper describes the first example of an adaption of near-field communication (NFC) technology—in 0.5 billion modern smartphones and mobile devices installed in 2014—toward portable, wireless, non-line-of-sight gas phase chemical sensing. We demonstrate the ability to convert inexpensive commercial NFC tags into chemical sensors that detect and discriminate analytes at part-per-thousand and part-per-million concentrations. This effort merges rational design of conductive nanostructured materials for selective chemical sensing with portable and widely distributed NFC technology to deliver a new method of acquiring chemical information about an NFC tag’s local environment. This paper introduces a concept for distributed chemical sensing by the growing number of people that carry NFC-enabled smartphones, tablets, and other smart devices. Chemical sensing is of critical importance to human health, safety, and security, yet it is not broadly implemented because existing sensors often require trained personnel, expensive and bulky equipment, and have large power requirements. This study reports the development of a smartphone-based sensing strategy that employs chemiresponsive nanomaterials integrated into the circuitry of commercial near-field communication tags to achieve non-line-of-sight, portable, and inexpensive detection and discrimination of gas-phase chemicals (e.g., ammonia, hydrogen peroxide, cyclohexanone, and water) at part-per-thousand and part-per-million concentrations.

Ultratrace Detection of Toxic Chemicals: Triggered Disassembly of Supramolecular Nanotube Wrappers.

Chemical sensors offer opportunities for improving personal security, safety, and health. To enable broad adoption of chemical sensors requires performance and cost advantages that are best realized from innovations in the design of the sensing (transduction) materials. Ideal materials are sensitive and selective to specific chemicals or chemical classes and provide a signal that is readily interfaced with portable electronic devices. Herein we report that wrapping single walled carbon nanotubes with metallo-supramolecular polymers creates sensory devices with a dosimetric (time- and concentration-integrated) increase in electrical conductivity that is triggered by electrophilic chemical substances such as diethylchlorophosphate, a nerve agent simulant. The mechanism of this process involves the disassembly of the supramolecular polymer, and we demonstrate its utility in a wireless inductively powered sensing system based on near-field communication technology. Specifically, the dosimeters can be powered and read wirelessly with conventional smartphones to create sensors with ultratrace detection limits.

Wireless Hazard Badges to Detect Nerve-Agent Simulants.

Human exposure to hazardous chemicals can have adverse short- and long-term health effects. In this Communication, we have developed a single-use wearable hazard badge that dosimetrically detects diethylchlorophosphate (DCP), a model organophosphorous cholinesterase inhibitor simulant. Improved chemically actuated resonant devices (CARDs) are fabricated in a single step and unambiguously relate changes in chemiresistance to a wireless readout. To provide selective and readily manufacturable sensor elements for this platform, we developed an ionic-liquid-mediated single walled carbon nanotube based chemidosimetric scheme with DCP limits of detection of 28 ppb. As a practical demonstration, an 8 h workday time weighted average equivalent exposure of 10 ppb DCP effects an irreversible change in smartphone readout.

Study of Two Papyrus Fragments with Fourier Transform Infrared Microspectroscopy

GJW The fragment is predominantly composed of oxidized cellulosic material, which is consistent with old papyrus. The fragment is largely homogenous in chemical composition. We found one anomalous feature that we were unable to identify. We did not observe any major spectral differences between “bare” papyrus and papyrus coated with ink. We did not observe any major spectral differences between the recto and verso sides of the papyrus fragment. The degree of oxidation is similar to that of the John fragment; however, the GJW fragment appears to be slightly less oxidized overall than the John fragment. Oxidation of the fragments is dependent on both their storage conditions and their ages, among other factors.