@article{li_freeman_boyter_qian_2015, title={One-Step Pad Dyeing and DP Finishing of Cotton: Part 1. Reactive Dyes with DMDHEU}, volume={2}, ISSN={["2330-5517"]}, DOI={10.14504/ajr.2.3.2}, abstractNote={One-step dyeing and durable press (DP) finishing offers potential advantages such as energy savings, reduced production time, and quick response to the market. In the present research, six reactive dyes were used in combination with DMDHEU, a DP finishing agent, in one-step and conventional two-step dyeing and finishing processes. Colorfastness properties and DP ratings of fabrics treated by the one-step dyeing and finishing process were comparable to those fabrics dyed and finished in separate steps.}, number={3}, journal={AATCC JOURNAL OF RESEARCH}, author={Li, Shiqi and Freeman, Harold S. and Boyter, Henry, Jr. and Qian, Lei}, year={2015}, pages={6–12} }
 @article{li_freeman_boyter_2015, title={One-Step Pad Dyeing and DP Finishing of Cotton: Part 2. Mechanism of Dye Fixation Using DMDHEU}, volume={2}, ISSN={["2330-5517"]}, DOI={10.14504/ajr.2.3.3}, abstractNote={This paper is a follow up to previous work from these laboratories, which led to a method for simultaneous reactive dye fixation and DMDHEU finishing of cotton at significantly higher shade depths (K/S values) than previously reported. The introduction of a steaming step prior to curing was critical to achieving high shade depths. The goal of this report is to present the mechanistic basis for these results. In this regard, results from conducting reactive dye/DMDHEU chemistry on a solid surface and from solvent extractions of dyed cotton before and after powdering indicate that dye fixation occurred by DMDHEU-induced entrapment rather than dye-fiber dye-DMDHEU bond formation.}, number={3}, journal={AATCC JOURNAL OF RESEARCH}, author={Li, Shiqi and Freeman, Harold S. and Boyter, Henry, Jr.}, year={2015}, pages={13–20} }
 @misc{boumaza_moretti_dizene_2014, title={Numerical simulation of flow and mixing in ROCOM facility using uniform and non-uniform inlet flow velocity profiles}, volume={280}, ISSN={["0029-5493"]}, DOI={10.1016/j.nucengdes.2014.10.018}, abstractNote={Water loss and depressurization of the primary circuit of a PWR lead to the actuation of the safety injection system (ECC). The cold water injected in the cold legs of the primary circuit is mixed partially with high temperature water. The cold water may cause a thermal shock to the reactor pressure vessel (RPV). The latter is more severe if the safety injection water enters the reactor vessel without mixing beforehand. The simulation and assessment of the mixing can be made using CFD codes. In the present framework, three-dimensional simulations are carried out using the CFD code ANSYS CFX, to investigate the mixing phenomenon in the Rossendorf Coolant Mixing Model (ROCOM) test facility. The predicted flow vertical velocity and tracer concentration distributions are presented and compared to the experimental data. Furthermore, the impact of the inlet velocity profile on the numerical results is assessed. The present results seem to confirm the capability of the CFD modeling to simulate the mixing phenomenon, which remains a key parameter for predicting the whole RPV behavior under abnormal cooling conditions.}, journal={NUCLEAR ENGINEERING AND DESIGN}, author={Boumaza, M. and Moretti, F. and Dizene, R.}, year={2014}, month={Dec}, pages={362–371} }
 @inproceedings{li_boyter_2010, title={Applications of UV curing on textiles}, booktitle={Proceedings of the Second International Conference on Advanced Textile Materials & Manufacturing Technology}, author={Li, S. G. and Boyter, H.}, year={2010}, pages={336–343} }
 @article{li_lewis_stewart_qian_boyter_2008, title={Effect of finishing methods on washing durability of microencapsulated aroma finishing}, volume={99}, ISSN={["0040-5000"]}, DOI={10.1080/00405000701489701}, abstractNote={Abstract To achieve a durable aroma finish on textiles has been a long time dream for textile chemists. As fragrances are volatile, only microencapsulated aroma can stay on textiles for long periods, since capsules greatly reduce the aroma evaporation rate. An aroma finished textile has to be washable. Therefore, aroma capsules finished on textiles should not only last for long time statically but also withstand harsh washing conditions. Due to low affinity between encapsulated aroma and fabric, a fixing agent must be applied with the capsules; the fabric has to undergo a curing treatment to make the agent fix these capsules. However, the curing process is usually a high-temperature thermal procedure that causes aroma loss from capsules by quick evaporation. Thus, fragrant durability on fabrics can vary significantly with different fixing agents and curing processes. Three fixing agents, three kinds of thermal curing equipment, and various curing conditions were investigated. By analysing properties of the fixing agents, heat transfer characteristics of the curing apparatus, and delivered energies in the curing conditions, a washing durable aroma capsule finishing process for cotton fabric was developed.}, number={2}, journal={JOURNAL OF THE TEXTILE INSTITUTE}, author={Li, Shiqi and Lewis, Joy E. and Stewart, Neil M. and Qian, Lei and Boyter, Henry}, year={2008}, pages={177–183} }
 @article{smith_o'neal_boyter_pisczek_2007, title={Decolorizing textile dye wastewater by anoxic/aerobic treatment}, volume={82}, ISSN={["0268-2575"]}, DOI={10.1002/jctb.1629}, abstractNote={A method of biologically decolorizing wastewater from fiber reactive dyeing of cotton by sequential anoxic/aerobic treatment steps using a single biomass has been developed and evaluated for chemical oxygen demand and color removal. A viable biomass that effectively removes both color and chemical oxygen demand in a sequential anoxic/aerobic treatment process has been developed. This method may be retrofitted to existing aerobic wastewater treatment systems that are typically used to treat dyeing wastewater. Copyright © 2006 Society of Chemical Industry}, number={1}, journal={JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY}, author={Smith, Brent and O'Neal, Gilbert and Boyter, Henry and Pisczek, Jamie}, year={2007}, month={Jan}, pages={16–24} }
 @article{boyter_2007, title={Environmental legislation USA}, ISBN={["978-1-84569-115-8"]}, ISSN={["2042-0803"]}, DOI={10.1533/9781845693091.30}, number={66}, journal={ENVIRONMENTAL ASPECTS OF TEXTILE DYEING}, author={Boyter, H. A.}, year={2007}, pages={30–43} }
 @inproceedings{boyter_2007, title={Sustainabilility - just a PR gimmick?}, booktitle={Fashion garment washing: trends, fabrics, technologies & sustainability :  AATCC symposium ; December 12 - 13, 2007, Renaissance Hotel, Long Beach, California}, publisher={Research Triangle Park, NC:  AATCC}, author={Boyter, H.}, year={2007} }
 @article{li_boyter_2005, title={Washfastness improvement for heavy shade microdenier nylon 6,6 fabric}, volume={5}, number={8}, journal={AATCC Review}, author={Li, S. Q. and Boyter, H.}, year={2005}, pages={36–40} }
 @article{washfastness improvement for heavy shade microdenier nylon 6,6, fabric_2005, volume={5}, number={8}, journal={AATCC Review}, year={2005}, pages={36–40} }
 @inproceedings{effect of finishing methods on washing durability of microencapsulated fragrant finishing_2004, booktitle={Proceedings of the annual international conference & exhibition of AATCC :  September 13-17, 2004}, publisher={[Research Triangle Park, N.C.]:  AATCC}, year={2004} }
 @article{li_boyter_stewart_2004, title={Ultraviolet (UV) curing processes for textile coloration}, volume={4}, number={8}, journal={AATCC Review}, author={Li, S. and Boyter, H. and Stewart, N.}, year={2004}, pages={44–49} }
 @article{boyter_shoup_1988, title={A USEFUL SUBLIMATION AND SHORT-PATH DISTILLATION APPARATUS}, volume={65}, ISSN={["0021-9584"]}, DOI={10.1021/ed065p631}, abstractNote={ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTA useful sublimation and short-path distillation apparatusHenry A. Boyter and Willy Shoup Cite this: J. Chem. Educ. 1988, 65, 7, 631Publication Date (Print):July 1, 1988Publication History Received3 August 2009Published online1 July 1988Published inissue 1 July 1988https://doi.org/10.1021/ed065p631Request reuse permissionsArticle Views174Altmetric-Citations-LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (447 KB) Get e-Alertsclose Get e-Alerts}, number={7}, journal={JOURNAL OF CHEMICAL EDUCATION}, author={BOYTER, HA and SHOUP, W}, year={1988}, month={Jul}, pages={631–631} }
 @article{boyter_grimes_1988, title={NIDO-CARBORANE BUILDING-BLOCK REAGENTS .2. BULKY-SUBSTITUENT (ALKYL)2C2B4H6 DERIVATIVES AND (C6H5)2C2B4H6 - SYNTHESIS AND PROPERTIES}, volume={27}, ISSN={["0020-1669"]}, DOI={10.1021/ic00291a007}, abstractNote={The preparation and chemistry of nido-2,3-R/sub 2/C/sub 2/C/sub 2/B/sub 4/H/sub 6/ carboranes in which R is n-butyl, isopentyl, n-hexyl, and phenyl was investigated in order to further assess the steric and electronic influence of the R groups on the properties of the nido-C/sub 2/B/sub 4/ cage, especially with respect to metal complexation at the C/sub 2/B/sub 3/ face and metal-promoted oxidative fusion. The three dialkyl derivatives were prepared from the corresponding dialkylacetylenes via reaction with B/sub 5/H/sub 9/ and triethylamine, but the diphenyl compound could not be prepared in this manner and was obtained instead in a thermal reaction of B/sub 5/H/sub 9/ with diphenylacetylene in the absence of amine. All four carboranes are readily bridge-deprotonated by NaH in THF, and the anions of the dialkyl species, on treatment with FeCl/sub 2/ and air oxidation, generate the respective R/sub 4/C/sub 4/B/sub 8/H/sub 8/ carborane fusion products were R = n-C/sub 4/H/sub 9/, i-C/sub 5/H/sub 11/ or n-C/sub 6/H/sub 13/. The diphenylcarborane anion Ph/sub 2/C/sub 2/B/sub 4/H/sub 5//sup /minus// did not form detectable metal complexes with Fe/sup 2+/, Co/sup 2+/, or Ni/sup 2+/, and no evidence of a Ph/sub 4/C/sub 4/B/sub 8/H/sub 8/ fusion product has been found. Treatment of Ph/submore » 2/C/sub 2/B/sub 4/H/sub 6/ with Cr(CO)/sub 6/ did not lead to metal coordination of the phenyl rings, unlike (PhCH/sub 2/)/sub 2/C/sub 2/B/sub 4/H/sub 6/, which had previously been shown to form mono- and bis(tricarbonylchromium) complexes. However, the reaction of Ph/sub 2/C/sub 2/B/sub 4/H/sub 5//sup /minus//, CoCl/sub 2/, and (PhPCH/sub 2/)/sub 2/ did give 1,1-(Ph/sub 2/PCH/sub 2/)/sub 2/-1-Cl-1,2,3-Co(Ph/sub 2/C/sub 2/B/sub 4/H/sub 4/), the only case in which metal complexation of the diphenylcarborane was observed. 14 references, 3 figures, 3 tables.« less}, number={18}, journal={INORGANIC CHEMISTRY}, author={BOYTER, HA and GRIMES, RN}, year={1988}, month={Sep}, pages={3075–3079} }
 @article{boyter_grimes_1988, title={NIDO-CARBORANE BUILDING-BLOCK REAGENTS .3. CYCLIC AND OPEN-CHAIN OLIGOMERS INCORPORATING -CB4H6C- UNITS - CROWN CARBORANES}, volume={27}, ISSN={["0020-1669"]}, DOI={10.1021/ic00291a008}, abstractNote={The open-chain dialkynes EtC/identical to/C(CH/sub 2/)/sub n/C/identical to/CEt (n = 4, 6), the trialkyne HC/identical to/C(CH/sub 2/)/sub 5/C/identical to/CH, and the cyclic dialkynes CH/sub 2/(CH/sub 2/)/sub 4/C/identical to/C(CH/sub 2/)/sub n/C/identical to/C (n = 4-6) were treated with B/sub 5/H/sub 9/ and (C/sub 2/H/sub 5/)/sub 3/ to give the corresponding nido-carborane oligomers, in which the original -C/identical to/C- units are converted to -CB/sub 4/H/sub 6/C- nido-carborane cages. In each case, all available -C/identical to/C- groups were transformed to carborane moieties. No partially converted products (having both carborane and -C/identical to/C- groups in the chain) were found; when the B/sub 5/H/sub 9//-C/identical to/C- ratio employed was < 1, only completely converted products and unreacted starting materials were recovered at the end of the reaction. The open-chain carborane oligomers are viscous air-sensitive liquids that under undergo bridge deprotonation on treatment with NaH in THF solution; with excess NaH, one proton per carborane unit is removed. The resulting ionic species undergo complexation with Fe/sup 2+/ and oxidative fusion, forming products incorporating C/sub 4/B/sub 8/ cages. The cyclic bis(carborane) CH/sub 2/(CH/sub 2/)/sub 4/CB/sub 4/H/sub 6/C(CH/sub 2/)/sub 5/CB/sub 4/H/sub 6/C is an air-stable oil that can be deprotonated but does not under metal-promoted oxidative fusion. Allmore » products were characterized by /sup 11/B and /sup 1/H NMR, infrared, visible-uv, and mass spectroscopy, and the /sup 13/C NMR spectra of linear bis(carboranes) are reported. 9 references, 7 figures, 4 tables.« less}, number={18}, journal={INORGANIC CHEMISTRY}, author={BOYTER, HA and GRIMES, RN}, year={1988}, month={Sep}, pages={3080–3084} }
 @article{boyter_swisher_sinn_grimes_1985, title={7-VERTEX PHOSPHINOHALOMETALLACARBORANES OF IRON, COBALT, AND NICKEL - SYNTHESES, STRUCTURES, AND REACTIONS}, volume={24}, ISSN={["0020-1669"]}, DOI={10.1021/ic00217a023}, abstractNote={ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSeven-vertex phosphinohalometallacarboranes of iron, cobalt, and nickel: syntheses, structures, and reactionsHenry A. Boyter Jr., Robert G. Swisher, Ekk Sinn, and Russell N. GrimesCite this: Inorg. Chem. 1985, 24, 23, 3810–3819Publication Date (Print):November 1, 1985Publication History Published online1 May 2002Published inissue 1 November 1985https://doi.org/10.1021/ic00217a023Request reuse permissionsArticle Views49Altmetric-Citations34LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (1 MB) Get e-AlertscloseSupporting Info (1)»Supporting Information Supporting Information Get e-Alerts}, number={23}, journal={INORGANIC CHEMISTRY}, author={BOYTER, HA and SWISHER, RG and SINN, E and GRIMES, RN}, year={1985}, pages={3810–3819} }