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Dive into the research topics where Joseph F. Stanzione is active.

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Featured researches published by Joseph F. Stanzione.


Chemsuschem | 2012

Lignin Model Compounds as Bio-Based Reactive Diluents for Liquid Molding Resins

Joseph F. Stanzione; Joshua M. Sadler; John J. La Scala; Richard P. Wool

Lignin is a copious paper and pulping waste product that has the potential to yield valuable, low molecular weight, single aromatic chemicals when strategically depolymerized. The single aromatic lignin model compounds, vanillin, guaiacol, and eugenol, were methacrylated by esterification with methacrylic anhydride and a catalytic amount of 4-dimethylaminopyridine. Methacrylated guaiacol (MG) and methacrylated eugenol (ME) exhibited low viscosities at room temperature (MG: 17 cP and ME: 28 cP). When used as reactive diluents in vinyl ester resins, they produced resin viscosities higher than that of vinyl ester-styrene blends. The relative volatilities of MG (1.05 wt% loss in 18 h) and ME (0.96 wt% loss in 18 h) measured by means of thermogravimetric analysis (TGA) were considerably lower than that of styrene (93.7 wt% loss in 3 h) indicating the potential of these chemicals to be environmentally friendly reactive diluents. Bulk polymerization of MG and ME generated homopolymers with glass transition temperatures (T(g)s) of 92 and 103 °C, respectively. Blends of a standard vinyl ester resin with MG and ME (50 wt % reactive diluent) produced thermosets with T(g)s of 127 and 153 °C, respectively, which are comparable to vinyl ester-styrene resins, thus demonstrating the ability of MG and ME to completely replace styrene as reactive diluents in liquid molding resins without sacrificing cured-resin thermal performance.


Green Chemistry | 2012

Vanillin-based resin for use in composite applications

Joseph F. Stanzione; Joshua M. Sadler; John J. La Scala; Kaleigh H. Reno; Richard P. Wool

Lignin is an abundant, renewable material that has the potential to yield valuable, low molecular weight, single aromatic chemicals when strategically depolymerized. In order to generate a highly bio-based thermoset for use in polymer composites, a lignin-derived chemical, vanillin, was methacrylated in a two-step, one-pot synthesis to produce a vinyl ester resin (87 cP at 25 °C) with a 1 : 1 mole ratio of a mono-functional monomer, methacrylated vanillin, to cross-linking agent, glycerol dimethacrylate. The synthetic scheme was solventless, required little catalyst and moderate reaction temperatures while generating no by-products. Upon resin curing, a hard, transparent thermoset with a broad glass transition, Tg = 155 °C (based on the tan δ maximum), and a temperature of maximum decomposition rate, Tmax, of 426 °C was produced. Overall, a potentially 100% bio-based thermoset was synthesized possessing comparable thermo-gravimetric and thermo-mechanical properties to commercial vinyl ester-based thermosets.


International Journal of Environmental Research and Public Health | 2016

Experimental Data Extraction and in Silico Prediction of the Estrogenic Activity of Renewable Replacements for Bisphenol A.

Huixiao Hong; Benjamin G. Harvey; Giuseppe R. Palmese; Joseph F. Stanzione; Hui Wen Ng; Sugunadevi Sakkiah; Weida Tong; Joshua M. Sadler

Bisphenol A (BPA) is a ubiquitous compound used in polymer manufacturing for a wide array of applications; however, increasing evidence has shown that BPA causes significant endocrine disruption and this has raised public concerns over safety and exposure limits. The use of renewable materials as polymer feedstocks provides an opportunity to develop replacement compounds for BPA that are sustainable and exhibit unique properties due to their diverse structures. As new bio-based materials are developed and tested, it is important to consider the impacts of both monomers and polymers on human health. Molecular docking simulations using the Estrogenic Activity Database in conjunction with the decision forest were performed as part of a two-tier in silico model to predict the activity of 29 bio-based platform chemicals in the estrogen receptor-α (ERα). Fifteen of the candidates were predicted as ER binders and fifteen as non-binders. Gaining insight into the estrogenic activity of the bio-based BPA replacements aids in the sustainable development of new polymeric materials.


International Journal of Biological Macromolecules | 2018

Incorporating allylated lignin-derivatives in thiol-ene gel-polymer electrolytes

Elyse A. Baroncini; Joseph F. Stanzione

Growing environmental and economic concerns as well as the uncertainty that accompanies finite petrochemical resources contributes to the increase in research and development of bio-based, renewable polymers. Concurrently, industrial and consumer demand for smaller, safer, and more flexible technologies motivates a global research effort to improve electrolytic polymer separators in lithium-ion batteries. To incorporate the aromatic structural advantages of lignin, a highly abundant and renewable resource, into gel-polymer electrolytes, lignin-derived molecules, vanillyl alcohol and gastrodigenin are functionalized and UV-polymerized with multi-functional thiol monomers. The resulting thin, flexible, polymer films possess glass transition temperatures ranging from -42.1°C to 0.3°C and storage moduli at 25°C ranging from 1.90MPa to 10.08MPa. The crosslinked polymer films swollen with electrolyte solution impart conductivities in the range of 7.04×10-7 to 102.73×10-7Scm-1. Thiol molecular weight has the most impact on the thermo-mechanical properties of the resulting films while polymer crosslink density has the largest effect on conductivity. The conducting abilities of the bio-based gel-polymer electrolytes in this study prove the viability of lignin-derived feedstock for use in lithium-ion battery applications and reveal structurally and thermally desirable traits for future work.


Chemsuschem | 2018

Towards Sustainable High-Performance Thermoplastics: Synthesis, Characterization, and Enzymatic Hydrolysis of Bisguaiacol-Based Polyesters

Silvio Curia; Antonino Biundo; Isabel Fischer; Verena Braunschmid; Georg M. Gübitz; Joseph F. Stanzione

The utilization of wood-derived building blocks (xylochemicals) to replace fossil-based precursors is an attractive research subject of modern polymer science. Here, we demonstrate that bisguaiacol (BG), a lignin-derived bisphenol analogue, can be used to prepare biobased polyesters with remarkable thermal properties. BG was treated with different activated diacids to investigate the effect of co-monomer structures on the physical properties of the products. Namely, derivatives of adipic acid, succinic acid, and 2,5-furandicarboxylic acid were used. Moreover, a terephthalic acid derivative was used for comparison purposes. The products were characterized by 1 H NMR spectroscopy, attenuated total reflectance FTIR spectroscopy, gel-permeation chromatography, thermogravimetric analysis, and differential scanning calorimetry to assess their structural and thermal properties in detail. The polymers showed glass-transition temperatures ranging up to 160 °C and thermal stabilities in excess of 300 °C. Furthermore, the susceptibility of the polyester to enzymatic hydrolysis was investigated to assess the potential for further surface functionalization and/or recycling and biodegradation. Indeed, hydrolysis with two different enzymes from the bacteria Thermobifida cellulosilytica led to the release of monomers, as quantified by HPLC. The results of this study indicate that our new polyesters represent promising renewable and biodegradable alternatives to petroleum-based polyesters currently employed in the plastics industry, specifically for applications in which high-temperature stability is essential to ensure overall system integrity.


Archive | 2016

An Edible Education in Sustainable Development: Investigating Chocolate Manufacturing in a Laboratory-Based Undergraduate Engineering Course

Alexander Vincent Struck Jannini; Christian M. Wisniewski; Mary M. Staehle; Joseph F. Stanzione; Mariano J. Savelski

Green engineering, sustainability, and sustainable development are topics of great import to all engineering disciplines. To introduce students to these topics, hands-on experiments were developed for inclusion within a multi-disciplinary freshman engineering course. In these experiments, students learned to produce chocolate truffles and, ultimately, challenged to analyze and optimize the sustainability of the process with a cradle-to-gate and social life cycle assessments. Student analyses incorporated waste management strategies, overall energy and material consumption calculations, carbon reduction strategies, the use of engineering software, and the importance of fair trade in this industry. Eighty-nine freshman engineering students at Rowan University completed the experiments. Pre- and post-tests were used to evaluate the effectiveness of the course on increasing student knowledge of sustainability, of sustainable development, and of the impact engineers can have on socioeconomics. Preliminary results indicate that the course was effective in enhancing student knowledge and awareness of the social and environmental implications of chocolate manufacturing. A complete analysis and description are presented in this paper.


ACS Sustainable Chemistry & Engineering | 2013

Lignin-Based Bio-Oil Mimic as Biobased Resin for Composite Applications

Joseph F. Stanzione; Philip A. Giangiulio; Joshua M. Sadler; John J. La Scala; Richard P. Wool


ACS Sustainable Chemistry & Engineering | 2014

A Facile Method for Generating Designer Block Copolymers from Functionalized Lignin Model Compounds

Angela L. Holmberg; Joseph F. Stanzione; Richard P. Wool; Thomas H. Epps


Journal of Applied Polymer Science | 2016

Recent advances in bio‐based epoxy resins and bio‐based epoxy curing agents

Elyse A. Baroncini; Santosh Kumar Yadav; Giuseppe R. Palmese; Joseph F. Stanzione


ACS Sustainable Chemistry & Engineering | 2016

Synthesis and Characterization of Bio-based Epoxy Resins Derived from Vanillyl Alcohol

Eric Hernandez; Alexander W. Bassett; Joshua M. Sadler; John J. La Scala; Joseph F. Stanzione

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