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Vinyl acetate

Vinyl acetate is a colorless, flammable liquid with a sweet odor.
It is used in the production of various polymers and copolymers, including polyvinyl acetate, polyvinyl alcohol, and ethylene-vinyl acetate.
These materials have a wide range of applications, such as in adhesives, coatings, textiles, and packaging.
Reasearch into the synthesis, properties, and uses of vinyl acetate is an important area of study in chemistry and materials science.
PubCompare.ai's AI-powered platform can help optimize your vinyl acetate research by locating the best protocols from literature, preprints, and patents, using intelligent comparisons to ensure reproducibility and accuracy.
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Most cited protocols related to «Vinyl acetate»

Stearic acid and SPAN 80 were purchased from Merck (Merck KGaA, Darmstadt, Germany). Arachidic acid, Tween 60, Tween 80, poly(vinyl alcohol), L-lysine monohydrochloride, lithium carbonate, dansyl chloride, methylamine hydrochloride, triethylamine and sodium acetate were purchased from Sigma-Aldrich (St. Louis, MO, USA) and Miglyol 812 was purchased from Caelo (Caesar & Loretz GmbH, Hilden, Germany). Precirol ATO 5 and Compritol 888 ATO were kindly provided by Gattefossé (Saint Priest Cedex, France). L-Phenylalanine ethyl-ester hydrochloride was purchased from Fluka (Fluka Chemie GmbH, Buchs, Switzerland), acetic acid was obtained from VWR Chemicals (VWR International S.A.S., Fontenay-sous-Bois, France) and acetonitrile and methanol were obtained from Honeywell (Honeywell Riedel-de Häen AG, Seelze, Germany). Aqueous solutions were prepared with double-deionized water (Arium Pro, Sartorius AG, Göttingen, Germany).
Publication 2020
Acetic Acid acetonitrile arachidic acid Cedax Compritol ATO 888 dansyl chloride L-phenylalanine ethylester Lithium Carbonate Lysine Methanol methylamine hydrochloride miglyol 812 Polyvinyl Alcohol precirol ATO 5 Sodium Acetate Span 80 stearic acid triethylamine Tween 60 Tween 80
All participants wore standardised thin cotton socks with their most commonly used footwear during testing.
The five conditions analysed were: (Figure 1):
(i) Shoe alone (control),
(ii) Customised foot orthosis,
(iii)  Contoured polyethylene sham foot orthosis,
(iv) Contoured ethylene vinyl acetate (EVA) sham   foot orthosis,
(v)  Flat ethylene vinyl acetate (EVA) sham foot orthosis.
All feet were cast with the participant prone, using a commonly used technique to gain a neutral impression of the foot [25 (link)]. The customised foot orthosis was a modified Root style device balanced to the neutral calcaneal stance position as it is the most commonly prescribed orthosis by Australian and New Zealand podiatrists [25 (link)]. The orthotic shell thickness was either 3.0 mm, 4.0 mm or 4.5 mm polypropylene which was determined by each participant’s bodyweight and foot posture [17 (link)]. Participants with a neutral or pronated foot (FPI > 0) and bodyweight under 75 kg were prescribed a 4.0 mm polypropylene shell, while participants with a bodyweight 75 kg or over were prescribed a 4.5 mm shell. Participants with a cavoid foot (FPI < 0) were issued a 3.0 mm shell if their weight was less than 75 kg, while a 4.0 mm shell was issued if their weight was greater than 75 kg. Each customised foot orthosis was manufactured by a commercial orthotic laboratory (Footwork Podiatry Laboratory Pty Ltd, Melbourne, Australia) using a computer-aided design and computer-aided manufacturing process (CAD-CAM), whereby each orthosis was moulded against a positive cast that was milled from a timber composite block.
Following this, the two contoured sham orthoses were moulded against the same positive cast as the customised foot orthosis. One of the moulded sham devices was made from 1 mm polyethylene. The other moulded sham device was made from 3 mm EVA (90 kg/m2). These materials were chosen as both were expected to collapse under minimal force, thus providing minimal effect on plantar pressures (see Additional file 1: Figures S1 and S2 for basic information on the deformation characteristics of the foot orthoses). Both of these devices received minimal modification post-moulding, and the contoured orthosis had minimal grinding under the heel. The final flat sham orthosis was made from 3 mm EVA (90 kg/m2) and was only bevelled at the anterior margin just proximal to the metatarsophalangeal joint line. The contoured [14 (link),17 (link)] and flat EVA sham foot orthosis [10 (link)] were also selected as similar devices have been used in previous randomised controlled trials or trials in progress. All sham and customised orthoses were covered with the same thin vinyl material.
Publication 2013
Calcaneus CD3EAP protein, human Ethylenes Flatfoot Foot Foot Orthoses Gossypium Heel Medical Devices Metatarsophalangeal Joint Orthotic Devices Polyethylenes Polypropylenes Polyvinyl Chloride Shock Tooth Root vinyl acetate
Plant tissues were frozen in liquid nitrogen or placed in RNA stabilization reagent (RNA later™, Qiagen) and stored at -20°C before RNA extraction. Approximately 100 mg of plant tissues were crushed in liquid nitrogen with poly-vinyl-poly pyrrolidone. The powder was transferred in a tube containing 1 ml of extraction buffer " TE3D " (14.8 g EDTA, 84.4 g Tris, 20 g Nonidet P-40, 30 g lithium dodecyl sulfate, 20 g sodium deoxycholate, 95 ml H2O) [59 (link)]. After 15 min incubation at room temperature, 1 ml of sodium acetate (3 M) and one volume of chloroformisoamyl alcohol (24:1) were added. Purification of the aqueous phase was carried out following centrifugation by adding one volume of mixed alkyl tri-ethyl ammonium bromine solution (2% MATAB, 3 M NaCl) followed by 15 min at 74°C. The residual polysaccharides were then eliminated by addition of one volume of chloroformisoamyl alcohol (24:1) and centrifugation; the aqueous phase was precipitated by the addition of one volume of isopropyl alcohol. After centrifugation, the pellet was resuspended in 50 μl of ribonuclease free water containing 1 μl of ribonuclease inhibitor (RiboLock™, Fermentas).
RNA samples from cacao tissues were isolated following the procedure of Charbit et al [59 (link)] with modifications. Following DNase treatment (DNase I, Fermentas), RNA was then extracted with the phenolchloroformisoamyl alcohol (25:24:1) step and precipitated with one-tenth volume of 3 M sodium acetate, pH 5.3, and 2.5 volumes of 100% ethyl alcohol. An aliquot of RNA was then run by elecrophoresis on a 1.2% agarose gel and stained with ethidium bromide to confirm RNA integrity.
Publication 2008
2-pyrrolidone Ammonium Bromine Buffers Cacao Centrifugation Deoxycholic Acid, Monosodium Salt Deoxyribonuclease I Deoxyribonucleases dodecyl sulfate, lithium salt Edetic Acid Ethanol Ethidium Bromide Freezing Isopropyl Alcohol Nitrogen Nonidet P-40 Plants Poly A Polysaccharides Polyvinyl Chloride Powder Ribonucleases Sepharose Sodium Acetate Sodium Chloride Tissues Tromethamine
For evaluating the flame retardancy performance of polymers, one may need to visualize the hidden phenomena behind fire scenarios. For example, THR has a unit of energy, but TTI is the time scale that demonstrates the resistance of the system against the appearance of flame at the initial stage of a fire. Therefore, they are inherently of a different nature and cannot be considered alone or in combination as a good criterion for evaluating the flame retardancy of thermoplastic composites. The other difficulty with measuring fire retardancy performance is that the situation of interaction of additives with polymers is always unknown. Hirschler [6 (link)] defined “Fire Performance Index”, FPI, in brief, as the ratio of the TTI to the pHRR having the unit of sm2/kW. The FPI appeared as a first-order indicator of tendency to flashover. The higher FPI values could principally specify a higher fire retardancy performance when a higher numerator, a lower denominator, or both moving in the aforementioned directions could be observed. A lower pHRR was simultaneously required for achieving higher performance levels. A wide variety of systems have been studied and concluded that such an approach would be a good measure for flame retardancy assessment. Nevertheless, one may need a simpler way to evaluate the function of flame retardants used in thermoplastic composites, such as a dimensionless criterion which could eliminate the need for simultaneous evaluation of two different measures with their own dimensions each reflecting a complexity of explanation. The new criterion had to be simple, universal, including three main parameters (pHRR, THR and TTI), and critically dimensionless to image the fingerprint of fire in a given thermoplastic composite.
To develop the idea that a universal dimensionless index is necessary, there is a perquisite to distinguish one thermoplastic composite from the other in terms of flame retardancy performance. Following the first steps taken in the aforementioned study, the plot of THR (MJ/m2) (Y-axis) versus pHRR/TTI (kW/m2.s) (X-axis) could be considered as a new pattern of fire retardancy performance. The lower X and Y axes were looked for when expecting a higher performance from a thermoplastic composite. In this sense, a huge body of literature was searched to find thermoplastic composites in which only one kind of additive was used. To give the research a versatile character, four types of polymer matrices were selected among different families of thermoplastic: polypropylene (PP) as a commodity highly flammable polymer, poly(methyl methacrylate) (PMMA) as an engineering polymer, poly(lactic acid) (PLA) as a biopolymer, and poly(ethylene-co-vinyl acetate) (EVA) as an emerging polymer widely used in the cable industry. Table 1 summarizes the whole data extracted from the literature on cone calorimetry features of selected systems.
The variations of THR versus pHRR/TTI for the composites based on PP, PMMA, EVA, and PLA are then presented in Figure 2. This figure visualizes the actions of additives of different types and families in the aforementioned thermoplastic matrixes for evaluating the flame retardancy behavior of composites. Two points should be cared when using these plots. First, since data are picked out from different sources considering the limited access to reports in which the desired cone calorimetry data could be extracted from, each plot for the assigned thermoplastic contains several symbols denoting the mentioned neat polymer. The diversity of flame retardancy levels of neat polymers in each plot is an indication of the difference in flame retardancy of the selected polymer matrix in terms of molecular weight and viscosity obviously controlled over flame retardancy behavior of the specified thermoplastic. Second, the distribution pattern of flame retardancy of thermoplastic composites featured by THR (MJ/m2) and pHRR/TTI (kW/m2.s) in any specified case can be detected with symbols of spread positions in the area of the plot that can be noticed as a signature of complexity of the behavior of system against fire. The mauve arrows in the plots represent the direction toward which a desired flame retardancy improvement was likely to ensue. When THR and pHRR/TTI together take a low value, the desired flame retardancy will be recognized. However, the comparison is qualitative and there is no measure for quantifying the performance of systems. In other words, the unanswered question remaining with such a qualitative plot is: “Which polymer matrix or flame retardant additive would be the best choice?” The main complexity of providing an answer to the above question is that the very broad distribution of symbols (assigned to additives marked in each plot) gives a complex nature to the performance of flame retardant additives, each with its own hidden effect on the fire behavior of the system, and they cannot explicitly be held responsible for their actions.
Here, we define and put into practice the "Flame Retardancy Index”, FRI, as a simple yet universal dimensionless index in terms of pHRR, THR, and TTI. The FRI was defined as the ratio of THR*(pHRRTTI) between the neat polymer and the corresponding thermoplastic composite containing only one flame retardant additive: Flame Retardancy Index (FRI)=[THR * (pHRRTTI)]Neat Polymer[THR * (pHRRTTI)]Composite
In principal, it is expected that by introducing the flame retardant additive and dividing the term calculated for the neat polymer to that of the thermoplastic composite, a dimensionless quantity greater than 1 is obtained. This operation and incorporation of a neat polymer value in the FRI formula lets us compare the different systems regardless of the nature of the used polymer in terms of molecular weight or viscosity. Having this in mind and by calculating FRI for reliable data on thermoplastic systems given in Table 1, we defined “Poor”, “Good”, and “Excellent” fire retardancy features assigned to well-classified ranges of FRI quantities colored in red, blue, and green, respectively (Figure 3). Classically saying, the quality of the flame retardancy performance can be assigned to the quantitative levels defined below in terms of ranges in FRI values (Figure 3). It is expected to see the value of 100 from Equation (1) as the low limit for flame retardancy performance below which the addition of a flame retardant additive is not reasonable. This is representative of a system in which the addition of a flame retardant additive inversely affects performance. Therefore, FRI < 1 is taken as the lowest level of flame retardancy symbolized as “Poor” performance. Since data are gathered from a variety of reports in which different polymers (PP, PLA, PMMA, and EVA) filled with different amounts of various additives are included, the trend in the variation pattern of FRI can be considered as a snapshot of the behavior of thermoplastic composites when subjected to fire. From Figure 3A it can be observed that FRI values up to 101 (1 ˂ FRI ˂ 10) are the most probable case, which are nominated as the “Good” zone colored in blue. A closer view of “Poor” and “Good” situations is provided in Figure 3B. The majority of FRI values calculated by Equation (1) are located in between 1 and 10. Moreover, in contrast to our initial expectation, some FRI values took quantities below 100. This suggests that flame retardants can also contribute to combustion and, therefore, even in the presence of a flame retardant, the flame retardancy of a polymer can be worsened. The FRI values between 101 and below 102 (10 ˂ FRI ˂ 100) are labeled “Excellent” and are distinguished by a green background in Figure 3A. Three points are located in the excellent flame retardancy zone. These systems contain EVA and expanded graphite [12 (link)] or zinc borate [11 (link)]. Expanded graphite is well known as a conventional flame retardant that acts on the barrier effect of a formed char, in terms of quality and quantity, during the combustion. It can also change the thermal conductivity of a polymer. Its incorporation into polymer leads to the increase of thermal conductivity and, therefore, to the dissipation of heat at the surface of the polymer. It is worth mentioning that the loading percentage of expanded graphite is unusually and extremely high for this type of flame retardant in the aforementioned study [12 (link)]. Zinc borate is a char promoter and during the degradation, forms compact char, which protects the underlying polymer from fire. Once again, in this study, the incorporation percentage of zinc borate is higher than the usual quantity [24 (link)].
The dimensionless index nominated as FRI is useful for the comparative evaluation of the flame retardancy performance of thermoplastic systems regardless of the types of polymers and additives used. However, for now, this index is only adapted to simple fire scenarios where one peak of HRR appears during combustion. More complex fire scenarios can happen when two or more pHRR are compared to a second curve. In that case, one may need a high flame resistance rather than flame retardancy and, therefore, the char quantity and quality should be meticulously considered as well.
Publication 2019
Body temperature was recorded during three winter seasons (2009/10, 2012/13, 2013/14) using temperature data loggers (iButtons, DS1922L-F5#, range: −40 to +85 °C, accuracy: ±0.5 °C, Maxim Integrated Products International, Dublin, Ireland). The iButtons (coated in Elvax ethylene vinyl acetate resins, DuPont, and paraffin, gas-sterilised; potted mass: ~4.5 g) were implanted subcutaneously in the neck region (dorsal, between the scapulae). This method has proved successful in this species due to the absence of pronounced prehibernation fattening (Hufnagl et al. 2011 ; Lebl and Millesi 2008 ). Individuals were trapped in the early morning hours and transported (~20 min) to a veterinary clinic where the implantation was done under isoflurane anaesthesia. When the animals had recovered from anaesthesia, they were returned to the field site and released at their burrows, i.e., about 1–2 h after trapping and still within their daily morning activity period (Schmelzer and Millesi 2005 ). In total, we implanted 36 hamsters with iButtons. The burrows of the implanted individuals were monitored weekly during winter (open/closed) to detect potential activity. None of the individuals showed signs of above-ground activity until mid-March. Starting in early March, burrows of implanted individuals were checked at daily intervals, active hamsters were recaptured, and the data loggers were removed using the above-mentioned techniques. We were able to recover iButtons of 28 individuals (recovery rate: 78 %). None of the recaptured animals lost the data logger during winter, but two iButtons failed (one of an adult male and one of an adult female). Thus, temperature data of five adult males, seven adult females, eight juvenile males, and six juvenile females were analyzed in this study. Body mass and overwinter survival rates of implanted individuals did not differ from untreated ones of the same age and sex (Siutz et al. unpublished data). Emergence date was defined as the date when an individual was observed above ground or trapped for the first time (this was also the day when an individual removed its burrow plug). Emergence body mass was used for analysis when measured within 1 week after the individual’s vernal emergence date. Mass changes over winter were calculated as percentage of differences between immergence and emergence body mass.
Body temperature was recorded at 90-min intervals from autumn until recapture of individuals in spring. Torpor bouts were defined as multiday periods of reduced body temperature between two arousals, from the sampling interval when body temperature started to continuously decrease from 30 °C to at least 15 °C until it had reached 30 °C again. To analyze hibernation patterns, we defined the following parameters: hibernation onset (date of the first torpor bout), duration of post-immergence euthermy (days spent euthermic after immergence until hibernation onset), number of torpor bouts, mean torpor bout duration (calculated in hours, expressed as days), time spent in torpor (total duration of all torpor bouts, calculated in hours, expressed as days), mean arousal bout duration (calculated in hours, expressed as days), hibernation end (date of the last torpor bout), hibernation duration (days from the onset of the first and termination of the last torpor bout), and duration of preemergence euthermy (days spent euthermic after termination of the last torpor bout until vernal emergence).
Publication 2016
Adult Anesthesia Animals Arousal Body Temperature Elvax ethylene Females Hamsters Hibernation Human Body Isoflurane Males Natural Springs Neck Ovum Implantation Paraffin Resins, Plant Scapula vinyl acetate Woman

Most recents protocols related to «Vinyl acetate»

The stearate-coated
bCC/ethylene vinyl acetate compounds were prepared
according to an industrial procedure. Briefly, polymers and raw materials,
in the right mass ratio, were cold introduced into a closed mixer
(Comerio Ercole S.p.A.). Through friction, the mixture reached the
temperature of 90 °C and then was discharged into the hopper
of a granulation extruder (Filmex SAS). Successively, the granules
were introduced into the hopper of an injection press (Main Group),
plasticized at 95 °C, and injected into the mold at about 200
°C, where the expansion and cross-linking reactions took place
for a curing time of about 7 min. The specimens were cooled in a temperature-controlled
environment at 23 °C and stored at the same temperature.
Publication 2024
Not available on PMC !
PVAc gels were prepared from PVA gels by acetylation in a mixture of acetic anhydride (40 vol %)-acetic acid (10 vol %)-pyridine (50 vol %) at 90 °C for 8 h. The details of the Scheme 1 Cross-linking of dissolved PVA chains with glutaradehyde in the presence of HCl chemical procedure have been discussed in previous publications [15, 19, 20] . The gel samples were washed with toluene. The extent of acetylation was measured and an agreement within 1 to 2% was found between the calculated and experimentally determined values. The dry PVAc networks were swollen in isopropyl alcohol.
Publication 2024
Acrylic acid and n-butanol were obtained from Sigma Aldrich. Toluene, methyl alcohol, diethyl ether, p-Toluene sulfonic acid and Hydroquinone were obtained from Alfa Aesar. Commercial Ethylene Vinyl Acetate (EVA) copolymer with = 28 wt. % of vinyl acetate (VA) content was purchased from ExxonMobil Chemical Company. Lastly, crude oil was obtained from the western desert of Egypt (QN field — Qarun Company), with a physiochemical characteristic listed in Table 1.

Physiochemical characteristics of crude oil.

TestMethodResults
[email protected] ℃, g/LASTM D-12980.79
Specific gravity@60/60 ℉ASTM D-40520.79
API gravity@60 ℉ASTM D-405247.08
Viscosity kinematics at 40 ℃ cStASTM D-4453.33
Pour point (℃)ASTM D-9715
Wax content (wt.%)UOP 46/644.67
Asphaltene content (wt.%)IP 143/570.3
Ash content (wt.%)IP 4/940.001
Carbon residue (wt.%)IP 13/940.44
Sulfur content (wt.%)ASTM D-42940.09
Water content (vol%)IP 74/700.01
Flash point (℃)IP 170− 19
Gross calorific value (MJ/Kg)ASTM D-24046.37
Publication 2024
Copper sulfate pentahydrate was obtained from El-Goumhouria Co., Cairo, Egypt. Ascorbic acid was obtained from Merck Chemical Co., Germany. Tween 80 surfactant (T80) was obtained from MP Biomedical Co., India. Low density polyethylene pellets were obtained from El Sewedy Plastic Manufacturing (SEDPLAST), Tenth of Ramadan City, Cairo, Egypt. Ethylene vinyl acetate containing 18% of vinyl acetate was obtained from Arkema Inc., North America. Bidistalled water was utilized throughout the preparation steps.
Publication 2024
All chemicals in this study were obtained from commercial sources and did not require further purification. Lipase TL IM form Thermomyces lanuginosus was purchased from Novo Nordisk. Adenosine was purchased from Macklin (Shanghai, China), inosine was purchased from Accela (Shanghai, China), 6-chloropurine nucleoside was purchased from Aladdin (Shanghai, China). Vinyl acetate was purchased from SCRC (Shanghai, China), vinyl laurate from Aladdin (Shanghai, China), vinyl palmitate and divinyl adipate from TCI (Tokyo, Japan). Harvard Instrument PHD 2000 syringe pump was purchased from Harvard University (Holliston, MA, USA). The flow reactor and Y-mixer were purchased from Beijing Haigui Medical Engineering Design Co., Ltd. (Beijing China). A 400 MHz NMR spectrometer (Billerica, MA, USA) were also used in this study.
Publication 2024

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Polyvinyl alcohol is a synthetic, water-soluble polymer. It is commonly used as a raw material in the production of various laboratory equipment and supplies.
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Vinyl acetate is a chemical compound used in the production of various polymers and resins. It serves as a building block for the synthesis of materials such as polyvinyl acetate, polyvinyl alcohol, and ethylene-vinyl acetate copolymers. The core function of vinyl acetate is to provide a versatile raw material for the manufacturing of these important industrial and commercial products.
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Acetonitrile is a colorless, volatile, flammable liquid. It is a commonly used solvent in various analytical and chemical applications, including liquid chromatography, gas chromatography, and other laboratory procedures. Acetonitrile is known for its high polarity and ability to dissolve a wide range of organic compounds.
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Ethyl acetate is a clear, colorless liquid solvent commonly used in laboratory applications. It has a characteristic sweet, fruity odor. Ethyl acetate is known for its ability to dissolve a variety of organic compounds, making it a versatile tool in chemical research and analysis.
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Sodium hydroxide is a chemical compound with the formula NaOH. It is a white, odorless, crystalline solid that is highly soluble in water and is a strong base. It is commonly used in various laboratory applications as a reagent.
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DMSO is a versatile organic solvent commonly used in laboratory settings. It has a high boiling point, low viscosity, and the ability to dissolve a wide range of polar and non-polar compounds. DMSO's core function is as a solvent, allowing for the effective dissolution and handling of various chemical substances during research and experimentation.
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Dichloromethane is a clear, colorless, and volatile liquid commonly used as a laboratory solvent. It has a molecular formula of CH2Cl2 and a molar mass of 84.93 g/mol. Dichloromethane is known for its high solvent power and low boiling point, making it suitable for various laboratory applications where a versatile and efficient solvent is required.
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Methanol is a clear, colorless, and flammable liquid that is widely used in various industrial and laboratory applications. It serves as a solvent, fuel, and chemical intermediate. Methanol has a simple chemical formula of CH3OH and a boiling point of 64.7°C. It is a versatile compound that is widely used in the production of other chemicals, as well as in the fuel industry.

More about "Vinyl acetate"

polyvinyl acetate, polyvinyl alcohol, ethylene-vinyl acetate, Kollidon® VA64, acetonitrile, ethyl acetate, sodium hydroxide, hydrochloric acid, DMSO, dichloromethane, methanol