Polyvinyl Acetate and Vinyl Acetate-Ethylene Hybrid Adhesive: Synthesis, Characterization, and Properties

The goal is to develop a hybrid IPN network of polyvinyl acetate (PVAc) and ethylene-vinyl acetate (VAE). In this research work, the vinyl acetate (VAc)/ VAE hybrid emulsion and polyvinyl acetate emulsion (PVAc) were effectively synthesized. Emulsions with various characteristics have been developed by adjusting the weight ratios between the vinyl acetate monomer and the VAE component. The impacts on the mechanical, thermal, and physical properties of the films were investigated using tests for pencil hardness, tensile shear strength, pH, contact angle measurement, differential scanning calorimetry (DSC), and viscosity. When 5.0 weight percent VAE was added, the tensile shear strength in dry conditions decreased by 18.75% after a 24-hour bonding period, the heat resistance decreased by 26.29% (as per WATT 91) and the tensile shear strength decreased by approximately 36.52% in wet conditions (per EN 204). The pristine sample’s results were also confirmed by the contact angle test. The interpenetrating network (IPN) formation in hybrid PVAc emulsion as primary bonds does not directly attach to PVAc and VAE chains. The addition of VAE reduced the mechanical properties (at dry conditions) and heat resistance as per WATT 91. Contact angle analysis demonstrated that PVAc adhesives containing VAE had increased water resistance when compared to conventional PVA stabilised PVAc homopolymer-based adhesives. When compared to virgin PVAc Homo, the water resistance of the PVAc emulsion polymerization was enhanced by the addition of VAE.

Regulating the Localization of Intumescent Flame Retardant for Improving the Flame Retardancy of Ethylene-vinyl Acetate Copolymer Using Polyamide 6 as a Charring Agent

Polyamide 6 (PA6) was employed as a charring agent of intumescent flame retardant (IFR) to improve the flame retardancy of ethylene-vinyl acetate copolymer (EVA). Different processing procedures were used to regulate the localization of IFR in the EVA matrix. Localizations in which IFR was dispersed in the PA6phase or in the EVA phase were prepared. The effect of the localization of IFR on the flame retardancy of EVA was investigated. The limited oxygen index (LOI), vertical burning (UL 94) and cone calorimeter test (CCT)showed that the localization of IFR in the EVA matrix exhibited a remarkable influence on the flame retardancy.Compared with EVA/IFR, a weak improvement in the flame retardancy was observed in the EVA/PA6/IFR blend withthe localization of IFR in the PA6 phase. When IFR was regulated from the PA6 phase to the EVA matrix,a remarkable increase in the flame retardancy was exhibited. The LOI was increased from 27.8%to 32.7%, and the UL 94 vertical rating was increased from V-2 to V-0. Moreover, an approximately 41.36%decrease in the peak heat release rate was exhibited. A continuous and compact intumescent charring layer that formed in the blends with the localization of IFR in the EVA matrix should be responsible for its excellent flame retardancy.

Studies on the Simultaneous Synthesis of Dimethyl Carbonate and Poly(ethylene terephthalate): I. Catalytic Activity of Metal Acetate in Transesterification of Ethylene Carbonate with Dimethyl Terephthalate

A novel direct method for preparation of dimethyl carbonate and poly（ethylene terephthalate） from ethylene carbonate and dimethyl terephthalate has been demonstrated in the presence of metal acetate catalysts, lithium acetate dihydrate showed highest catalytic activity with 47.9% yield of dimethyl carbonate. This method was a green chemical process.

Synthesis of Acetic Acid on Pd-H_4SiW_(12)O_(40)-Based Catalysts by Direct Oxidation of Ethylene

Synthesis of acetic acid by direct oxidation of ethylene on Pd-H4SiW12O40-based catalysts was studied in a fixed-bed integral reactor and a pulse differential reactor. From the performance of the catalysts with different compositions and configurations, it is proposed that acetic acid is predominantly produced via an intermediate of acetaldehyde. This can be easily confirmed by comparing the product distributions in the integral and the differential reactors. The active sites for acetic acid formation are considered to exist mainly at the boundaries between the H4SiW12O40 and the Pd particles. The Pd-based catalysts reduced by H2/N2 have higher activities than those reduced by hydrazine, as explained by the degree of Pd dispersion obtained from the characteristics of hydrogen chemical adsorption. It was found that the Pd-Se-SiW12/SiO2 catalyst with selenium tetrachloride as a precursor was more active than that with potassium selenite, and that the acetic acid yield can be greatly increased by adding a suitable amount of dichloroethane (C2H4C12/C2H4 mole ratio=0.03) to the reactants.

Transesterification of Ethylene Carbonate with Dimethyl Terephthalate over Various Metal Acetate Catalysts

The reaction between ethylene carbonate and dimethyl terephthalate was carried out for the simultaneous synthesis of dimethyl carbonate and poly（ethylene terephthalate）, This reaction is an excellent chemical process that is environmentally friendly and produces no poisonous substance. The metal acetate catalysts used for this reaction are discussed in detail. Lithium acetate dihydrate was found to be a novel and efficient catalyst for this reaction. Compared with other metal acetates, lithium acetate dihydrate can attain a maximum catalytic activity at a lower concentration. When the reaction was carried out under the following conditions： the reaction temperature from 230 to 250 ℃, molar ratio of ethylene carbonate（EC） to dimethyl terephthalate（DMT） 3： 1, reaction time 3 h, and a catalyst amount of 0. 4% （molar fraction to DMT）, the yield of dimethyl carbonate（DMC） was 79. 1%.

RING-OPENING COPOLYMERIZATION OF DL-LACTIDE AND POLY(ETHYLENE GLYCOL) INITIATED BY LANTHANUM ACETATE AND APPLICATION OF THE COPOLYMER AS MATRIX OF MICROSPHERES CONTAINING VIBRIO CHOLERA ANTIGENS

Poly-dl-lactide-poly(ethylene glycol) (PELA) triblock copolymers were synthesized with lanthanum acetate as the initiator. PELA microspheres with entrapped Vibrio Cholera antigen and outer membrane protein (OMP) were prepared by a double emulsion W/O/W based on solvent extraction methods. The obtained microspheres showed smooth and spherical surface and their size varied between 0.5 and 5.0 mu m, which are suitable for oral targeting delivery system. The distribution tests in rabbits and mice through scanning electronic micrography and fluorescence microscope indicated that microspheres have successfully reached the immunization-related tissues, such as the liver, spleen and intestinal peyer's patches, following oral administration. The PELA microspheres were also evaluated as an efficient antigen delivery system by enhancing a higher protective ratio against live Vibrios Cholera.

Intercalation of multiply solvated hexafluorophospate anion into graphite electrode from mixtures of methyl acetate,ethyl methyl and ethylene carbonates

Graphite is a universal host material for ion intercalation. Li+-graphite intercalation compounds (GICs) have been successfully utilized as the anode material in commercial lithium-ion batteries.Similarly, anion-graphite intercalation compounds (AGICs) have been coming into their own in dual-ion batteries [1]. It is imperative to deepen an understanding of anion storage mechanisms in graphite electrode.

Sound Absorption Properties of Discarded Feathers/Ethylene Vinyl Acetate Copolymer Thermoplastic Composite Materials

The discarded feathers / ethylene vinyl acetate copolymer( EVA) thermoplastic composite materials was obtained with discarded feathers as reinforced material and EVA powders as matrix material by hot pressing method. Sound absorption properties were studied by changing mass ratio of discarded feathers and EVA,thickness of composite materials,hot pressing pressure and hot pressing temperature. It was found that the sound absorption properties of composite materials were good when the mass ratio of discarded feathers and EVA was 1: 1,thickness of composite materials was 30 mm,hot pressing pressure was 8 MPa,and hot pressing temperature was 80 ℃. Under the optimum conditions,the effect of composite density on sound absorption property was analyzed. In a certain range,the sound absorption property was enhanced with the decrease of the composite density.When the composite density was 0. 1g /cm^3, the maximum absorption coefficient was 0.96. Finally,the capillary theory was used to calculate the maximum sound absorption coefficient of discarded feathers / EVA thermoplastic composite materials. The good agreements of experimental results and calculated results proved the validity of the theoretical models.

Polyvinyl acetate/poly(amide-12-b-ethylene oxide) blend membranes for carbon dioxide separation

In this paper,blend membranes from polyvinyl acetate(PVAc)and block copolymer poly(amide-12-b-ethylene oxide)(Pebax1074)are prepared by solution casting and solvent evaporation method.Although they are homogeneous on a macro-scale,the observations from DSC and SEM indicate micro-phase separation for PVAc/Pebax1074 blend membranes.With the increase of Pebax1074 content,gas permeabilities of CO2,H2,N2and CH4all increase greatly.PVAc/Pebax1074 blend membranes with high PVAc content are appropriate for CO2/CH4separation.The temperature dependence of gas permeability is divided into rubbery region and glassy region.The activation energies of permeation in rubbery region are smaller than those in glassy region,and they all decrease with increasing Pebax1074 content.For N2,H2and CH4,their gas permeation properties are mainly influenced by the dual-mode sorption and hydrostatic pressure effect.But for CO2,its permeability increases with the increase of pressure due to CO2-induced plasticization effect,which is more obvious for PVAc/Pebax1074 blend membranes with high PVAc content.

Effect of ethylene vinyl acetate content on the performance of VMD using HDPE co-blending membrane

Membranes were fabricated with high-density polyethylene (HDPE) and ethylene vinyl acetate (EVA) blend through thermally induced phase separation and were then used for vacuum membrane distillation (VMD). The membranes were supported by non woven polyester fabric with a special cellular structure. Different membrane samples were obtained by adjusting the polymer concentration, HDPE/EVA weight ratio, and coagulation bath temperature. The membranes were characterized by scanning electron microscopy (SEM) analysis, contact angle test, and evaluation of porosity and pore size distribution. A series of VMD tests were conducted using aqueous NaCI solution (0.5 mol·L^-1) at a feed temperature of 65 ℃ and permeate side absolute pressure of 3 kPa. The membranes showed excellent performance in water permeation flux, salt rejection, and long-term sta-bility. The HDPE/EVA co-blending membranes exhibited the largest permeation flux of 23.87 kg·m^-2·h^-1, and benign salt rejection of ≥99.9%.

Preparation of Ethylene Glycol Monoethyl Ether Acetate Using a Tubular Reactor

Ethylene glycol monoethyl ether acetate (EGEA), an excellent solvent, is prepared with ethylene oxide (EO) and ethyl acetate (EA) in a tubular reactor under suitable reaction condition. The single circulation yield can reach 81%. This technology is not only safe but also makes it possible to continuously produce EGEA in industry,with low content of high boiling point by-products.

Sensing Property of Carbon Nanotube Yarn Embedded in Ethylene Vinyl Acetate (EVA) Elastomer

Carbon nanotube (CNT) has remarkable piezoresistive properties,which makes its extremely sensitive to the mechanical force. In this study,the CNT yarn with the strength of 90 MPa and the strain sensing gage factor of 1.75 was selected and embedded into the ethylene vinyl acetate (EVA) elastomer as a sensing material.By measuring the electric resistance changing under the stretching,bending,longitudinally and transversely compressing of the CNT embedded EVA, the resistance changing curves and their linear correlations were obtained and analyzed. The result shows that the gage factor under the tensile test is the highest( 2.51),which is higher than the original value of CNT yarn (1.75). The gage factors of the CNT yarn embedded into EVA elastomer under bending and longitudinal and transverse compression are 2.29,1.55 and 0.79,respectively.

Effects of Nano-Filler on the Thermal and Fire-Resistant Properties of Ethylene-Vinyl Acetate Copolymer

Sepiolite （S9, B10, B20, B40） and boehmite have been added to an intumecent flame retardant （IFR） system to produce the halogen-free and fire-resistant ethylene-vinyl acetate copolymer （EVM） rubber. The rubber contains ammonium polyphosphate （APP） as acid source, double pentaerythritol （D-PER） as carbon source and melamine （MN） as gas source. The effects of nano-filler sepiolite and boehmite on the fire-resistant property of EVM rubber based on IFR system were investigated. The test results show that the system with nano-filler of sepiolite B10 has the best fire-resistant property. The process of smoke emission and thermal decomposition, the element composition of char surface and the micro morphology of intumecent char layer of the EVM IFR system with nano-filler were also studied by NBS chamber, thermogravimetric （TG） analysis, X- ray photoelectron spectroscopy （XPS） and scanning electron microscope （SEM）.

Difference in Surface Roughness of Ethylene-Vinyl-Acetate Sheet before and after Application of Finishing Liquid

Surface texture of the mouthguard affects the sense of adaptation in the athlete and further affects hygiene. Therefore, finish polishing is extremely important. The aim of this study was to investigate the difference in the surface roughness after finishing polishing of ethylene-vinyl-acetate (EVA) sheets and after application of the finishing liquid, and to evaluate its effectiveness. Total of 48 specimens of EVA (3 × 3 mm) were divided into 4 groups according to polishing condition (control = unpolished;condition A = Robinson-brush;condition B = Lisko-Fine, and condition C = Mouthguard-wheel). Polishing was performed at low speed by using a straight headpiece. The rotation speeds were 5000, 4000 and 6000 rpm for condition A, B, and C, respectively. Next, a finishing liquid was applied to each specimen. For application, a cotton swab was used, and it was applied by three reciprocations. A non-contact surface shape measuring machine was used for measuring surface roughness;the measurement range is 1.65 mm and the resolution is 0.01 nm. The arithmetic average height (Sa) was measured. The differences in the surface roughness before and 15 min after the application of the finishing liquid were analyzed by two-way analysis of variance and Bonferroni’s multiple comparison tests. Surface roughness of the specimen before application became coarse in the order of control, condition C, B and A, and Sa was about 0.20, 1.98, 2.92, and 4.71 μm, respectively. The degree of reduction in roughness was about 1.0 μm or more than each polished state in conditions A and B. Condition C was not significantly different before and after application. No significant difference was observed between condition B and C after application. The results of this study showed that the surface roughness decreased due to the application of the finishing liquid when the surface roughness after finish polishing was about 2.0 μm or more.

Difference in Surface Roughness of Ethylene-Vinyl-Acetate Sheet before and after Application of Finishing Liquid: Part 2 Changes over Time in Surface Roughness

Surface texture of the mouthguard affects the sense of adaptation in the athlete and further affects hygiene. The aim of this study was to investigate the changes over time in surface roughness after finish polishing of ethylene vinyl acetate (EVA) sheets and before and after finishing liquid application, and to evaluate its effectiveness. Total of 160 specimens of EVA (3 × 3 mm) were divided into 4 groups according to polishing condition (control = unpolished;RB = Robinson-brush;LF = Lisko-Fine, and MW = Mouthguard-wheel). Polishing was performed at low speed by using a straight headpiece. The rotation speed was 5000, 4000 and 6000 rpm for RB, LF, and MW, respectively. Next, a finishing liquid was applied to each specimen. Changes over time in surface roughness before and after application of the finishing liquid were compared by a non-contact surface shape measuring machine. The arithmetic average height (Sa) was measured. The measurement time points were before application, immediately after application, and at 5, 10, and 15 min after application. The changes over time of the surface roughness of the sheet before and after application of the finishing liquid were analyzed by two-way analysis of variance and Bonferroni’s multiple comparison tests. Surface roughness of the specimen before application became coarse in the order of control;MW, LF and RB, and Sa were about 0.21 μm, 2.03 μm, 2.94 μm, and 4.72 μm, respectively. That showed the same order after finishing liquid application. Significant decrease in Sa for RB and LF were seen at 10 min after application and at 5 min after application, respectively. Sa of MW was not significantly different before and after application. The results of this study showed that a lubricity of about 1.0 μm increases within 5 - 10 min of application of finishing liquid, but in cases where polishing was performed to about 2.0 μm;the application of finishing liquid has no ef-fect.

Ethylenediaminetetraacetic Acid Chelation for Band Keratopathy before Ab Interno Glaucoma Surgery

An 87-year-old woman with primary open-angle glaucoma presented to our hospital. Although the combined cataract and minimally invasive glaucoma surgeries (MIGS) were an appropriate surgical option, the presence of band keratopathy made it difficult to perform ab interno glaucoma surgery in her right eye (OD);therefore, the corneal opacity was removed using ethylenediaminetetraacetic acid (EDTA) chelation procedure. One month after chelation, microhook ab interno trabeculotomy and cataract surgery were performed successfully. Clear intraoperative visualization of the angle structures is critical for the success of these MIGS procedures. In glaucomatous eyes that require MIGS, EDTA chelation is a good neoadjuvant therapy for coexisting band keratopathy.

小空腔内EVA发泡胶带的黏结性能和发泡行为研究

采用4,4-氧代双苯磺酰肼(OBSH)作为发泡剂、以过氧化苯甲酰(BPO)作为交联剂、C9树脂作为增黏剂制备了乙烯-乙酸乙烯酯(EVA)发泡胶带,研究组分对2D发泡胶带使用性能的影响和机理。结果表明,在合适的EVA/BPO/OBSH/C9(100/3/3/40)条件下,发泡胶带能够在170℃和205℃下发泡。发泡胶带具有良好的使用性能,膨胀率超过2倍,不发生挂流,表面平整。同时,发泡胶带的拉伸强度高于5 MPa,断裂伸长率超过240%,吸水率低于5%。

低温等离子体活化氯丁橡胶和乙烯-乙酸乙烯酯共聚物及其复配改性沥青的性能

为提升胶粉改性沥青的性能,以与基质沥青质量比为11/100的氯丁橡胶(CR)和3/100的乙烯-乙酸乙烯酯共聚物(EVA)为改性剂制备了改性沥青,采用低温等离子体活化CR/EVA以进一步提升复配改性沥青的性能,研究了单一改性、复配改性和低温等离子体活化复配改性沥青(A-CR/EVA-MA)的路用性能,并使用扫描电子显微镜、原子力显微镜和傅里叶变换红外光谱分析了各改性沥青的微观机理。结果表明,各改性沥青的路用性能均有提升,总体表现为活化复配改性优于复配改性和单一改性;A-CR/EVA-MA的针入度、软化点、延度、布氏黏度及抗车辙因子较基质沥青分别提升了46%、47%、95%、253%和278%,存储稳定性也得到了进一步提高;低温等离子体活化技术增加了改性剂的比表面积和表面官能团含量,提高了改性剂对沥青中轻质组分的吸附能力,促进了CR和EVA与沥青的紧密结合,有效提升了改性沥青的路用性能。

我国乙烯-醋酸乙烯树脂的市场分析

乙烯-醋酸乙烯(EVA)树脂是以乙烯和醋酸乙烯酯为原料,采用本体聚合法生产的一种高附加值产品。近年来,随着光伏、涂覆等领域需求的不断增长,我国EVA树脂行业发展迅速。2023年,我国EVA树脂生产能力达到2450 kt/a,表观消费量达到3249.4 kt,随着新建和扩建装置的建成投产,我国EVA树脂的生产能力不断增长,供需矛盾进一步得到缓解。文章分析了我国EVA树脂的供需现状,指出了未来的发展趋势,并提出了今后的发展建议。