Veneer-based structural wood composites are typically manufactured using phenol-formaldehyde resols (PF) that are formulated with wheat flour extender and organic filler. Considering that this technology is several decades old, it is surprising to learn that many aspects of the formulation have not been the subject of detailed analysis and scientific publication. The effort described here is part of a university/industry research cooperation with a focus on how the organic fillers impact the properties of the formulated adhesives and adhesive bond performance. The fillers studied in this work are derived from walnut shell (Juglans regia), alder bark (Alnus rubra), and corn cob (furfural production) residue. Alder bark and walnut shell exhibited chemical compositions that are typical for lignocellulosic materials, whereas corn cob residue was distinctly different owing to the high pressure steam digestion used in its preparation. Also, all fillers had low surface energies with dominant dispersive effects. Surface energy of corn cob residue was a little higher than alder bark and walnut shell, which were very similar. All fillers reduced PF surface tension with effects greatest in alder bark and walnut shell. Surface tension reductions roughly correlated to the chemical compositions of the fillers, and probably resulted from the release of surface active compounds extracted from the fillers in the alkaline PF medium. It was shown that viscoelastic network structures formed within the adhesive formulations as a function of shear history, filler type, and filler particle size. Relative to alder bark and walnut shell, the unique behavior of corn cob residue was discussed with respect to chemical composition. Alder bark and walnut shell exhibited similar effects with a decrease of adhesive activation energy. However, corn cob reside caused much higher adhesive activation energy. Alder bark exhibited significant particle size effects on fracture energy and bondline thickness, but no clear size effects on penetration. Regarding corn cob residue and walnut shell, particle size effects on fracture energy were statistically significant, but magnitude of the difference was rather small. Classified corn cob residue fillers all resulted in a similar bondline thickness (statistically no difference) that was different walnut shell. / Ph. D.

Formaldehyde, a hazardous and toxic substance, can be found in most resin treated durable press fabrics. The current formaldehyde regulations are limited to worker exposure in an industrial setting and the possibility of government regulation of formaldehyde release from textiles is of concern to the textile industry. The most common test of formaldehyde release used by the U.S. textile industry is the AATCC Test Method 112, a colorimetric determination based on the Hantzsh reaction between ammonia, formaldehyde, and acetylacetone. The chromophore formed is 3,5-diacetyl-1,4-dihydrolutidine (DDL). In the AATCC test the ammonia and acetylacetone are in the Nash reagent and the formaldehyde is extracted from the fabric by trapped steam. The formaldehyde in solution and the Nash reagent are mixed and the color developed. The purpose of this study was to determine if a more effective formulation of the Nash reagent than currently used by industry can be produced. The reaction between the Nash reagent and formaldehyde is first order in formaldehyde, therefore pseudo-first order kinetics was used as the basis of the study. Reagent effectiveness was determined by comparisons and calculations based on the molar extinction coefficient, maximum absorbance, and rate constant. The study was set up in phases to investigate the effect of different ammonia sources, the effects of varying concentrations of the reactant components, the effect of ageing, and the effect of different temperatures on the formation of DDL. In the final phase the best reformulated reagent was compared to the Nash reagent under the conditions of the AATCC Test Method 112. Several reformulations were found to be comparable to Nash, but none was found to be more effective in formaldehyde detection. This study has shown some of the complexities of the reaction and that the Nash reagent is not able to obtain 100% conversion of formaldehyde to DDL. Therefore, any test that uses the Nash reagent is underestimating the releasable formaldehyde concentration in the fabric. / Ph. D.

In today’s society, textile producers and manufacturers strive to use as little harmful chemicals as possible in their finishing of textiles. Though, producing a completely chemical free fabric is nearly impossible, many companies work actively to scan and evaluate alternatives to chemical substances that have a negative effect on the environment and the human health.Prior preparations for the practical part of this project were conducted in a literature study, which entailed studying articles based on similar projects. Practical information was attained from the mentors at IKEA and from contact with the suppliers of the tested resins. A study of alternative methods of testing the resistance to creasing of textiles was conducted to the benefit of IKEA. A practical evaluation of the smoothness appearance of the test specimens resulted in a development of this existing method.To reassure the quality of the scan, obtained resins weretreated on cellulosic weaves, and later on evaluated based on demands IKEA has for easy care treated textiles. The demands concerning the content of formaldehyde and the grade of smoothness appearance retained after ten washes where followed throughout the whole project. The evaluation was conducted based on several quality tests made on the treated weave. This resulted in a recommendation of four different resins for IKEA to further investigate. / Program: Textilingenjörsutbildningen

This work presents the development of a laser-induced fluorescence technique to measure atmospheric formaldehyde. In conjunction with the technique, the design of a compact, narrow linewidth, etalon-tuned titanium:sapphire laser cavity which is pumped by the second harmonic of a kilohertz Nd:YAG laser is also presented. The fundamental tunable range is from 690-1100 nm depending on mirror reflectivities and optics kit used. The conversion efficiency is at least 25% for the fundamental, and 2-3% for intracavity frequency doubling from 3.5-4W 532 nm pump power. The linewidth is < 0.1 cm-1, and the pulsewidth is 18 nsec. Also presented are observations of gas-phase sulfuric acid from the NEAQS-ITCT 2K4 (New England Air Quality Study Intercontinental Transport and Chemical Transformation) field campaign in July and August 2004. Sulfuric acid values are reported for a polluted environment and possible nucleation events as well as particle growth within the boundary layer are explored. Sulfate production rates via gas phase oxidation of sulfur dioxide are also reported. This analysis allows an important test of our ability to predict sulfuric acid concentration and probe its use as a fast time response photochemical tracer for the hydroxyl radical, OH. In comparison, the NASA time-dependent photochemical box model is used to calculate OH concentration. Nighttime H2SO4 values are examined to test our understanding of nocturnal OH levels and oxidation processes. In comparison, sulfuric acid from a large ground based mission in Tecámac, México (near the northern boundary of Mexico City) during MIRAGE-Mex field campaign (March 2006) is presented. The observations in conjunction with the NASA LARc Photochemical box model are used to explore ozone production, nitrate and sulfate formation, and radical levels and radical production rates during the day. The one minute observations of sulfuric acid, sulfur dioxide, and aerosol surface area were again used to calculate OH levels assuming steady state, and are in good agreement with observations of OH (R2 = 0.7). Photochemical activity is found to be a maximum during the morning hours, as seen in ozone and nitrate formation.

Le formaldéhyde (HCHO) est un polluant majeur de l’air intérieur. L’objectif de cette thèse est de réaliser les avancées scientifiques et technologiques nécessaires à l’obtention d’une méthode analytique basée sur un dispositif microfluidique de mesure du formaldéhyde dans l’air associant précision, sélectivité, rapidité d’analyse avec pour objectif majeur une autonomie suffisante sur de longues durées, typiquement un mois. Le principe de la méthode reposait initialement sur trois étapes clés, à savoir le piégeage du formaldéhyde gazeux en solution, la réaction du formaldéhyde avec un agent dérivatif, puis la détection du produit de dérivation par colorimétrie ou fluorimétrie. La méthode a finalement évolué vers seulement deux étapes distinctes grâce à l’utilisation d’un dispositif microfluidique innovant dans lequel le piégeage et la réaction ont lieu simultanément. L’étude des performances analytiques du dispositif a permis de valider la méthode développée pendant cette thèse. / Formaldehyde (HCHO) is a major pollutant in indoor air. The objective of this work is to realize the scientific and technological advances required to obtain an analytical method based on a microfluidic device to measure air formaldehyde combining precision, selectivity, analysis speed with for major objective a sufficient autonomy on a long time, typically one month. The principle of the method was initially based on three key steps, the gaseous formaldehyde uptake in solution, the formaldehyde derivatization reaction, then the detection of reaction product by colorimetry or fluorimetry. The method has finally advanced toward only two definite steps thanks to the use of an innovative microfluidic device in which uptake and reaction take place simultaneously. The study of analytical performances of the device allows to validate the method developedduring this work.

Formaldehyde is one of the most prevalent and toxic chemicals found indoors, where we spend ~90% of our lives. Chronic exposure to formaldehyde indoors, therefore, is of particular concern, especially for sensitive populations like children and infants. Unfortunately, no effective filtration control strategy exists for its removal. While research has shown that proteins in sheep's wool bind permanently to formaldehyde, the extent of wool's formaldehyde removal efficiency and effective removal capacity when applied in active filtration settings is unknown. In this research, wool capacity experiments were designed using a plug flow reactor and air cleaner unit to explore the capacity of wool to remove formaldehyde given different active filtration designs. Using the measured wool capacity, filter life and annual costs were modeled in a typical 50 m₃ room for a variety of theoretical filter operation lengths, air exchange rates, and source concentrations. For each case, annual filtration costs were compared to the monetary benefits derived from wool resale and from the reduction in cancer rates for different population types using the DALYs human exposure metric. Wool filtration was observed to drop formaldehyde concentrations between 60-80%, although the effective wool removal capacity was highly dependent on the fluid mechanics of the filtration unit. The air cleaner setup yielded approximately six times greater capacity than the small-scale PFR designed to mimic active filtration (670 [mu]g versus 110 [mu]g HCHO removed per g of wool, respectively). The outcomes of these experiments suggest that kinematic variations resulting from different wool packing densities, air flow rates, and degree of mixing in the units influence the filtration efficiency and effective capacity of wool. The results of the cost--benefit analysis show that for the higher wool capacity conditions, cost-effectiveness is achieved by the majority of room cases when sensitive populations like children and infants are present. However, for the average population scenarios, filtration was rarely worthwhile, showing that adults benefit less from reductions in chronic formaldehyde exposure. These results suggest that implementation of active filtration would be the most beneficial and cost-effective in settings like schools, nurseries, and hospitals that have a high percentage of sensitive populations. / text

Formaldehyde is a ubiquitous and hazardous indoor air pollutant and reducing concentrations in indoor environments is a public health priority. The goals of this doctoral work were to advance analytical methods for continuous monitoring of formaldehyde at very low concentrations (sub-20 ppb[subscript v]) and to improve fundamental, mechanistic understanding of how structural and chemical properties of activated carbon influence removal of formaldehyde from indoor environments. To achieve these goals, emerging sensor-based technology was evaluated for its ability to detect and quantify ppb[subscript v]-level formaldehyde concentrations on a continuous basis at relative humidity levels characteristic of residential indoor environments. Also, a combination of spectroscopic and selective titration techniques was employed to characterize molecular-level structural and chemical properties of traditional and chemically treated granular activated carbon (GAC). In addition to selecting two different commercially available GACs for study, design and preparation of a laboratory-prepared, chemically treated GAC was pursued to create nitrogen-doped GAC with desirable surface chemical properties. Performance of all GACs was evaluated with respect to formaldehyde removal through a series of packed bed column studies. With respect to continuous formaldehyde monitoring, a method detection limit for emerging sensor technology was determined to be approximately 2 ppb[subscript v], and for relative humidity levels characteristic of indoor environments (> 40%), quantitative, continuous formaldehyde measurements less than 10 ppb[subscript v] were robust. The two commercially available GACs tested were both capable of removing formaldehyde; however, the GAC with greater density of basic surface functional groups and greater electron-donating potential (Centaur) removed twice as much formaldehyde (on a GAC mass basis) as the less basic GAC (BPL). A laboratory-prepared GAC (BPL-N) was successfully created to contain pyridinic and pyrrolic nitrogen, which was associated with increased surface density of basic functional groups, as well as with increased electron-donating potential. BPL-N exhibited better removal capacity for formaldehyde than BPL and Centaur. Furthermore, packed bed column studies of BPL-N and BPL formaldehyde removal performance yielded evidence to support the hypothesis that electron-donating potential, especially nitrogen functional groups at the BPL-N surface, promote catalytic removal of gas-phase formaldehyde via oxidation. / text

Highly functionalized 5 or 6-membered nitrogen-containing heterocyclic moieties are highly prevalent in pharmaceuticals reagents, alkaloid natural products, organocatalysts, as well as useful building blocks in organic synthesis. Novel approaches to synthesizing these structures are sought therefore to maximize their accessibility. Within the well-established organic synthesis artillery, electrocyclic reactions serve as the predominant strategy to construct pyrrolidine and piperidine analogues. In this dissertation, the first stereocontrolled assembly of indolizidines from 2-allylic proline esters by aza-Prins reaction, and endo-selective synthesis of highly functionalized 5-vinylic pyrrolidines from benzylic and allylic azomethine ylide using novel [3+2] dipolar cycloaddition are described. These methodologies then culminate in a formal synthesis of Borreria alkaloid, borrecapine, by using an unprecedented sulfonyl group substituted dipolarophile. Finally, new directions in our laboratory to make pyrrolidine scaffolds are included in the last chapter of this thesis.

Formaldehyde is widely used fixative. Its advantages are low cost, simplicity of use and good fixation traits, which are fast tissue penetration, good preservation of morphological structures and compatibility with downstream histological applications. Formaldehyde disadvantages are negative effects on nucleic acids. Formaldehyde solutions modify primary structure of deoxyribonucleic acid (DNA), fragment DNA and create protein-DNA covalent bonds that hinder DNA isolation procedures. Level of negative effects of formaldehyde is dependent on many factors. Effect of formaldehyde chemical composition (formaldehyde dilution, presence of buffer or formic acid) and effect of fixation length were studied in this work. On DNA extracted from fixed tissues, DNA quantity and level of DNA fragmentation were studied by quantitative polymerase chain reaction, fluorescence assay for DNA quantification and by on- chip electrophoresis on bioanalyzer Agilent 2100. Quality and quantity of acquired DNA were tested by DNA profile determination for identification purposes using STR (short tandem repeats) analysis. Results show that of all tested fixatives, buffered 4% formaldehyde is the most suited solution in regards of sufficient amount of DNA and sufficient DNA quality. Other formaldehyde variants (non-buffered 4%...

Resíduos de formaldeído são descarregados de diversas formas no ambiente, resultantes de muitos processos industriais, e de seu uso como conservantes. A pesquisa por tecnologias adequadas para o tratamento de formaldeído aponta processos físico-químicos e biológicos, com atenção especial para os processos anaeróbios por constituírem sistemas compactos e de baixo consumo energético. No entanto, algumas lacunas presentes na pesquisa sobre tratamento anaeróbio de formaldeído e alguns pontos de discordância devem ser esclarecidos. Em muitos casos, esses resíduos são descartados de forma intermitente, motivando a opção por processos em batelada. Nesse contexto, o presente estudo avaliou a degradação de formaldeído em reator anaeróbio operado em bateladas seqüenciais, contendo biomassa imobilizada em espuma de poliuretano. O desempenho do reator foi monitorado para várias concentrações afluentes de formaldeído, variando de 31,6 a 1104,4 mg/L. Os resultados obtidos indicaram excelente estabilidade do reator e eficiência de remoção de formaldeído acima de 99%. Entretanto foi constatado acúmulo de matéria orgânica no efluente devido à presença de ácidos orgânicos, principalmente acético e propiônico. Essa constatação levanta um questionamento importante sobre a rota anaeróbia de degradação do formaldeído, que pode diferir substancialmente do que foi registrado na literatura. Os ácidos gerados não foram degradados pela biomassa exposta ao formaldeído, contudo poderiam ser facilmente removidos com a utilização de um reator em série com inoculo adaptado à remoção de ácidos orgânicos. / Formaldehyde residues are discharged into the environment in several different ways, as a result of several industrial processes, as well as its use as a preservative. Research for suitable technologies for treatment of formaldehyde points to physical-chemical and biological processes, with special attention to anaerobic processes, once they represent compact systems with low energy requirements. Nevertheless, some blank spaces still remaining in the research regarding anaerobic treatment of formaldehyde must be filled, and some points of disagreement must be clarified. In several cases, formaldehyde residues are discharged intermittently, favoring the choice of batch processes. In this context, the present study evaluated the degradation of formaldehyde in an anaerobic sequencing batch reactor, containing biomass immobilized in polyurethane foam matrices. Reactor performance was monitored for different influent formaldehyde concentrations, ranging from 31.6 to 1104.4 mg/L. Results obtained indicate excellent reactor stability and efficiency in formaldehyde removal above 99%. However, accumulation of organic matter was observed in the effluent, due to presence of non-degraded organic acids, especially acetic and propionic. This observation poses an important question regarding the anaerobic route of formaldehyde degradation, which might differ substantially from that reported in literature. The degradation of the generated products could occur in another reactor in serie containing biomass adapted to organic acids removal.