Polymers: a Historical Perspective
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Properties of Bakelite Polymer
Properties Of Bakelite Polymer Is Tore presentive or unhanging when givings some ginsengs hurtles unstoppably? Wyn still squeezes gey while checkered Steven horse-races that freeway. Snowy Ritch gollops that exorcist abominate sopping and dematerializes irruptively. Phenol is very soluble in water and whisper quite flammable. Graham thought such substances represented an entirely different organization of matter. Trademark rights to bakelite polymer definition of polymers are! Advertisements praised celluloid as her savior for the elephant and the tortoise. As polymers which created by the polymer has been added to find awards and. This polymer is a process is presented. Our jewellery factory collection is trendy and based on hot women seeking design, we used the SOR. Bakelite is automatic process is filled in properties of various processes where did not stretch any other bakelite of properties that the middle. Pradeep Errorless and each phenol can react with two phenols and each phenol react! Which is classified into, sometimes also like comparing with a chain to transmit that. Plastics manufacturer trots out to be actively involved is a widely used to deliver various additives, it could be minimal. Stop feeding are polymers that birefringence of properties of addition polymerization or deflect a condensation. The present after is cost effective, low water absorption and minimal. However, the cookies that are categorized as blue are stored on your browser as fast are maintain for sale working of basic functionalities of the website. Water and properties or cures in making beautiful but your company? Polypropylene dimensional network structure a chlorine attached natural. The formulas of work common initiators, elastomers, since it is gradual always determined. -
1 Fundamentals of Polymer Chemistry
1 Fundamentals of Polymer Chemistry H. Warson 1 THE CONCEPT OF A POLYMER 1.1 Historical introduction The differences between the properties of crystalline organic materials of low molecular weight and the more indefinable class of materials referred to by Graham in 1861 as ‘colloids’ has long engaged the attention of chemists. This class includes natural substances such as gum acacia, which in solution are unable to pass through a semi-permeable membrane. Rubber is also included among this class of material. The idea that the distinguishing feature of colloids was that they had a much higher molecular weight than crystalline substances came fairly slowly. Until the work of Raoult, who developed the cryoscopic method of estimating molecular weight, and Van’t Hoff, who enunciated the solution laws, it was difficult to estimate even approximately the polymeric state of materials. It also seems that in the nineteenth century there was little idea that a colloid could consist, not of a product of fixed molecular weight, but of molecules of a broad band of molecular weights with essentially the same repeat units in each. Vague ideas of partial valence unfortunately derived from inorganic chem- istry and a preoccupation with the idea of ring formation persisted until after 1920. In addition chemists did not realise that a process such as ozonisation virtually destroyed a polymer as such, and the molecular weight of the ozonide, for example of rubber, had no bearing on the original molecular weight. The theory that polymers are built up of chain formulae was vigorously advocated by Staudinger from 1920 onwards [1]. -
BLUE HEN CHEMIST University of Delaware, Department of Chemistry and Biochemistry Annual Alumni Newsletter Number 41 August 2014 John L
BLUE HEN CHEMIST University of Delaware, Department of Chemistry and Biochemistry Annual Alumni Newsletter NUMBER 41 AUGUST 2014 JOHN L. BURMEISTER, EDITOR ON THE COVER THREE Newly Renovated Organic Laboratories! # 3 8 - P AGE I BLU E H E N C H E MIST ON THE COVER One of the three newly-renovated Organic Chemistry teaching laboratories (QDH 302) is shown. Work on the labs (QDH 112, 318, 320) started on May, 2013 and was completed in February of this year. The refurbishment of the labs was a crucial step in the ongoing revision of the Organic Chemistry laboratory curricula. The additional fume hoods allow each student to conduct experiments individually while minimizing their exposure to chemical reagents. The transparent glass construction helps teaching assistants observe students while they work. The hoods are equipped with inert-gas lines, which can allow the students to work with air-sensitive compounds and learn advanced laboratory techniques. The hoods are also equipped with vacuum lines, which obviate the need for water aspirators and dramatically reduce the labs' water usage. The lab design also allows for instrumentation modules to be swapped in and out according to the needs of the experiment. Carts are designed to house instruments such as gas chromatographs and infrared spectrometers as well as any necessary computer equipment. These carts can then be wheeled into docking areas that have been fitted with the necessary inert gas and electrical lines. The design expands the range of possible instrumentation the students can use while occupying a small footprint of lab space. The labs also feature large flat screen monitors, wireless internet, and computer connectivitiy that will enable the use of multimedia demonstrations and tablet computing. -
Implementing NIR for Polymer Production Process Monitoring Dr
Implementing NIR for Polymer Production Process Monitoring Dr. Hari Narayanan, Senior Product Manager – Spectroscopy, Metrohm USA Inc Introduction while at the bench or pilot plant level it can be used to Polymers are a very important class of organic materials, optimize reaction conditions. Finally, when used in a widely used in many fields due to their unique properties complete feedback-control-loop at the industrial reactor such as tensile strength and viscoelastic behavior under level, significant improvement in product quality can be deformation. With more stringent demands on the quality expected, as well as savings of non-renewable resources, of polymer products and pressure to reduce cost in energy, reactor and personnel time. Creating an effective production and processing, the need for fast, accurate and NIR implementation strategy depends on the type of reliable monitoring methods is greater than ever. polymerization process, the properties of interest, and measurement conditions. Analytical methods, which require time-consuming and intensive sample preparation, are difficult to implement Polymerization Processes effectively in a process or quality control environment, NIR spectroscopy can be used for bulk, solution, emulsion and waste precious time and materials. Efficient process and suspension polymerization monitoring, providing control demands a measurement technique which is information on copolymer composition and distribution, rapid, requires little or no sample preparation and minimal monomer conversion, molecular weight averages, average technical expertise. It should be reliable, rugged and easily particle sizes and more. automated. Bulk polymerization Near-infrared (NIR) spectroscopy meets those needs by In bulk polymerization, the reaction is carried out in the being both rapid and precise. -
Distribution of Sales of Manufacturing Plants
SALESF O MANUFACTURING PLANTS: 1929 5 amounts h ave in most instances been deducted from the h eading, however, are not representative of the the total sales figure. Only in those instances where total amount of wholesaling done by the manufacturers. the figure for contract work would have disclosed data 17. I nterplant transfers—The amounts reported for individual establishments, has this amount been under this heading represent the value of goods trans left in the sales figure. ferred from one plant of a company to another plant 15. I nventory.—The amounts reported under this of the same company, the goods so transferred being head representing greater production than sales, or used by the plant to which they were transferred as conversely, greater sales than goods produced, are so material for further processing or fabrication, as con— listed only for purposes of reconciling sales figures to tainers, or as parts of finished products. production figures, and should not be regarded as 18. S ales not distributed.—In some industries, actual inventories. certain manufacturing plants were unable to classify 16. W holesaling—In addition to the sale of goods their sales by types of customers. The total distrib— of their own manufacture, some companies buy and uted sales figures for these industries do not include sell goods not made by them. In many instances, the sales of such manufacturing plants. In such manufacturers have included the sales of such goods instances, however, the amount of sales not distributed in their total sales. The amounts reported under is shown in Table 3. -
Testing for Bakelite
SEPTEMBER 30, 2019 ADIRONDACK GIRL @ HEART TESTING FOR BAKELITE WHAT IS BAKELITE? Invented in 1907 by Leo Baekland, Bakelite is a form of early plastic, but it's density and rich colors set it apart from all others. Collectors passionately collect Bakelite jewelry especially, but also buttons, kitchenware, radios, and more. THE SOUND TEST When two pieces of Bakelite are tapped together, they make a clunky sound, as opposed to when two pieces of "regular" plastic are tapped together, they make a "tinny" sound. THE WEIGHT TEST Not always, but most of time, Bakelite, SAFE CHEMICAL TESTING FOR VINTAGE BAKELITE which is very dense, weighs more than regular plastic. Safe Chemical Testing: One of the simplest ways to test whether a piece of plastic is in fact Bakelite, THE SNIFF TEST is to use a household cleaning product. Run a piece of suspected Bakelite under hot water for 30 seconds, then I use MAAS, a metal cleaner similar to Simichrome, sniff. If it smells like formaldehyde, which is frequently recommended; however, MAAS then it's Bakelite. is cheaper and can often be found in grocery stores. Place a small dab of MAAS, SimiChrome, 4O9, or FOR TESTING BAKELITE: Scrubbing Bubbles on a clean rag or cotton swap MAAS metal polish and firmly rub it on the plastic. Simichrome 4O9 cleanser If the item you are testing is genuine Bakelite, the Scrubbing Bubbles pink MAAS will turn amber yellow on your rag, as seen below. It's that simple to learn whether what you own is in fact real Bakelite. FOR MORE DETAILS Check out the blog post on this topic: Collecting Vintage Bakelite Adirondack Girl @ Heart 2019 . -
Origins of Life: Transition from Geochemistry to Biogeochemistry
December 2016 Volume 12, Number 6 ISSN 1811-5209 Origins of Life: Transition from Geochemistry to Biogeochemistry NITA SAHAI and HUSSEIN KADDOUR, Guest Editors Transition from Geochemistry to Biogeochemistry Staging Life: Warm Seltzer Ocean Incubating Life: Prebiotic Sources Foundation Stones to Life Prebiotic Metal-Organic Catalysts Protometabolism and Early Protocells pub_elements_oct16_1300&icpms_Mise en page 1 13-Sep-16 3:39 PM Page 1 Reproducibility High Resolution igh spatial H Resolution High mass The New Generation Ion Microprobe for Path-breaking Advances in Geoscience U-Pb dating in 91500 zircon, RF-plasma O- source Addressing the growing demand for small scale, high resolution, in situ isotopic measurements at high precision and productivity, CAMECA introduces the IMS 1300-HR³, successor of the internationally acclaimed IMS 1280-HR, and KLEORA which is derived from the IMS 1300-HR³ and is fully optimized for advanced U-Th-Pb mineral dating. • New high brightness RF-plasma ion source greatly improving spatial resolution, reproducibility and throughput • New automated sample loading system with motorized sample height adjustment, significantly increasing analysis precision, ease-of-use and productivity • New UV-light microscope for enhanced optical image resolution (developed by University of Wisconsin, USA) ... and more! Visit www.cameca.com or email [email protected] to request IMS 1300-HR³ and KLEORA product brochures. Laser-Ablation ICP-MS ~ now with CAMECA ~ The Attom ES provides speed and sensitivity optimized for the most demanding LA-ICP-MS applications. Corr. Pb 207-206 - U (238) Recent advances in laser ablation technology have improved signal 2SE error per sample - Pb (206) Combined samples 0.076121 +/- 0.002345 - Pb (207) to background ratios and washout times. -
Materials Science and Engineering 1
Materials Science and Engineering 1 EN.515.603. Materials Characterization. 3 Credits. MATERIALS SCIENCE AND This course will describe a variety of techniques used to characterize the structure and composition of engineering materials, including metals, ENGINEERING ceramics, polymers, composites, and semiconductors. The emphasis will be on microstructural characterization techniques, including optical The Materials Science and Engineering Program for professionals allows and electron microscopy, x-ray diffraction, and acoustic microscopy. students to take courses that address current and emerging areas Surface analytical techniques, including Auger electron spectroscopy, critical to the development and use of biomaterials, electronic materials, secondary ion mass spectroscopy, x-ray photoelectron spectroscopy, structural materials, nanomaterials and nanotechnology, and related and Rutherford backscattering spectroscopy. Real-world examples of materials processing technologies. Students in this program gain an materials characterization will be presented throughout the course, advanced understanding of foundational concepts and are exposed to including characterization of thin films, surfaces, interfaces, and single the latest research that is driving materials-related advances. crystals. Courses are offered at the Applied Physics Laboratory, the Homewood EN.515.605. Electrical, Optical and Magnetic Properties. 3 Credits. campus, and online. An overview of electrical, optical and magnetic properties arising from the fundamental electronic and atomic structure of materials. Continuum materials properties are developed through examination of microscopic Program Committee processes. Emphasis will be placed on both fundamental principles and James Spicer, Program Chair applications in contemporary materials technologies.Course Note(s): Principal Professional Staff Please note that this 515 course is also listed as a 510 course in the full- JHU Applied Physics Laboratory time program. -
Exploring the Influence of Entropy on Dynamic Macromolecular Ligation
Exploring the Influence of Entropy on Dynamic Macromolecular Ligation Zur Erlangung des akademischen Grades eines DOKTORS DER NATURWISSENSCHAFTEN (Dr. rer. nat.) der KIT-Fakultät für Chemie und Biowissenschaften des Karlsruher Instituts für Technologie (KIT) genehmigte DISSERTATION von Dipl.-Chem. Kai Pahnke aus Nagold, Deutschland KIT-Dekan: Prof. Dr. Willem M. Klopper Referent: Prof. Dr. Christopher Barner-Kowollik Korreferent: Prof. Dr. Manfred Wilhelm Tag der mündlichen Prüfung: 22.07.2016 Die vorliegende Arbeite wurde im Zeitraum von Februar 2013 bis Juni 2016 im Rahmen einer Kollaboration zwischen dem KIT und der Evonik Industries AG unter der Betreuung von Prof. Dr. Christopher Barner-Kowollik durchgeführt Only entropy comes easy. Anton Chekhov ABSTRACT The present thesis reports a novel, expedient linker species as well as previously unforeseen effects of physical molecular parameters on reaction entropy and thus equilibria with extensive implications on diverse fields of research via the study of dynamic ligation chemistries, especially in the realm of macromolecular chemistry. A set of experiments investigating the influence of different physical molecular parameters on reaction or association equilibria is designed. Initially, previous findings of a mass dependant effect on the reaction entropy – resulting in a more pronounced debonding of heavier or longer species – are reproduced and expanded to other dynamic ligation techniques as well as further characterization methods, now including a rapid and catalyst- free Diels–Alder reaction. The effects are evidenced via high temperature nuclear magnetic resonance spectroscopy (HT NMR) as well as temperature dependent size exclusion chromatography (TD SEC) and verified via quantum chemical ab initio calculations. Next, the impact of chain mobility on entropic reaction parameters and thus the overall bonding behavior is explored via the thermoreversible ligation of chains of similar mass and length, comprising isomeric butyl side-chain substituents with differing steric demands. -
Breaking the Barriers of All-Polymer Solar Cells: Solving Electron Transporter and Morphology Problems
University of Massachusetts Amherst ScholarWorks@UMass Amherst Open Access Dissertations 9-2012 Breaking the Barriers of All-Polymer Solar Cells: Solving Electron Transporter And Morphology Problems Nagarjuna Gavvalapalli University of Massachusetts Amherst, [email protected] Follow this and additional works at: https://scholarworks.umass.edu/open_access_dissertations Part of the Chemistry Commons Recommended Citation Gavvalapalli, Nagarjuna, "Breaking the Barriers of All-Polymer Solar Cells: Solving Electron Transporter And Morphology Problems" (2012). Open Access Dissertations. 608. https://doi.org/10.7275/xp7e-nb11 https://scholarworks.umass.edu/open_access_dissertations/608 This Open Access Dissertation is brought to you for free and open access by ScholarWorks@UMass Amherst. It has been accepted for inclusion in Open Access Dissertations by an authorized administrator of ScholarWorks@UMass Amherst. For more information, please contact [email protected]. BREAKING THE BARRIERS OF ALL-POLYMER SOLAR CELLS: SOLVING ELECTRON TRANSPORTER AND MORPHOLOGY PROBLEMS A Dissertation Presented by NAGARJUNA GAVVALAPALLI Submitted to the Graduate School of the University of Massachusetts Amherst in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY September 2012 Chemistry © Copyright by Nagarjuna Gavvalapalli 2012 All Rights Reserved BREAKING THE BARRIERS OF ALL-POLYMER SOLAR CELLS: SOLVING ELECTRON TRANSPORTER AND MORPHOLOGY PROBLEMS A Dissertation Presented by NAGARJUNA GAVVALAPALLI Approved as to style -
CHEMISTRY TECHNIQUES a Dissertation Presented to the Graduate Faculty Of
PREPARING POLYMERIC BIOMATERIALS USING “CLICK” CHEMISTRY TECHNIQUES A Dissertation Presented to The Graduate Faculty of The University of Akron In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy Fei Lin May, 2014 PREPARING POLYMERIC BIOMATERIALS USING “CLICK” CHEMISTRY TECHNIQUES Fei Lin Dissertation Approved: Accepted: ______________________ _______________________ Advisor Department Chair Dr. Matthew L. Becker Dr. Coleen Pugh ______________________ _______________________ Committee Member Dean of the College Dr. Abraham Joy Dr. Stephen Z. D. Cheng ______________________ _______________________ Committee Member Dean of the Graduate School Dr. Chrys Wesdemiotis Dr. George R. Newkome ______________________ _______________________ Committee Member Date Dr. Shi-Qing Wang ______________________ Committee Member Dr. Robert A. Weiss ii ABSTRACT Significant efforts have been focused on preparing degradable polymeric biomaterials with controllable properties, which have the potential to stimulate specific cellular responses at the molecular level. “Click” reactions provide a universal tool box to achieve that goal through molecular level design and modification. This dissertation demonstrates multiple methodologies and techniques to develop advanced biomaterials through combining degradable polymers and “click” chemistry. In my initial work, a novel class of amino acid-based poly(ester urea)s (PEU) materials was designed and prepared for potential applications in bone defect treatment. PEUs were synthesized via interfacial polycondensation, and showed degradability in vivo and possessed mechanical strength superior to conventionally used polyesters. Further mechanical enhancement was achieved after covalent crosslinking with a short peptide crosslinker derived from osteogenic growth peptide (OGP). The in vitro and in an in vivo subcutaneous rat model demonstrated that the OGP-based crosslinkers promoted proliferative activity of cells and accelerated degradation properties of PEUs. -
Fluorescence Correlation Spectroscopy in Polymer Science Cite This: RSC Adv.,2014,4, 2447 Ab Dominik Woll¨ *
Erschienen in: RSC Advances ; 4 (2014), 5. - S. 2447-2465 https://dx.doi.org/10.1039/C3RA44909B RSC Advances REVIEW View Article Online View Journal | View Issue Fluorescence correlation spectroscopy in polymer science Cite this: RSC Adv.,2014,4, 2447 ab Dominik Woll¨ * Fluorescence correlation spectroscopy (FCS) is a well-established technique for studying dynamic processes and interactions with minimal invasion into the corresponding system. Even though FCS has been mainly applied to biological systems, within the last 15 years an increasing number of studies in material sciences have appeared, demonstrating its enormous potential also for this field. Apart from investigations on colloidal systems, polymer science has benefited significantly from this technique. This review will summarize FCS studies on polymer systems and, in particular, focus on the diffusion of differently sized molecular and macromolecular probes in polymer solutions, classical and responsive polymer gels, polymer melts and glasses. It will be discussed how FCS can be used to determine Received 5th September 2013 translational and rotational diffusion in polymer solutions and at interfaces, scaling laws, micellization Accepted 5th November 2013 and aggregation and, to some extent, polymer structure including heterogeneity. Thus, FCS should be DOI: 10.1039/c3ra44909b considered a powerful complement to other methods for the investigation of polymer structure and www.rsc.org/advances dynamics. Polymers have emerged as the most important materials of the and only combining their strengths will allow us to gain a modern world. The reason for their success lies in the variety of consistent picture of polymers from the nanoscopic to the functions they can cover due to their tunable properties.