A Polyvinyl Alcohol/Acrylamide Hydrogel with Enhanced Mechanical Properties Promotes Full-Thickness Skin Defect Healing by Regulating Immunomodulation and Angiogenesis Through Paracrine Secretion

Hydrogel-based tissue-engineered skin has attracted increased attention due to its potential to restore the structural integrity and functionality of skin.However,the mechanical properties of hydrogel scaffolds and natural skin are substantially different.Here,we developed a polyvinyl alcohol(PVA)/acrylamide based interpenetrating network(IPN)hydrogel that was surface modified with polydopamine(PDA)and termed Dopa-gel.The Dopa-gel exhibited mechanical properties similar to native skin tissue and a superior ability to modulate paracrine functions.Furthermore,a tough scaffold with tensile resistance was fabricated using this hydrogel by three-dimensional printing.The results showed that the interpenetration of PVA,alginate,and polyacrylamide networks notably enhanced the mechanical properties of the hydrogel.Surface modification with PDA endowed the hydrogels with increased secretion of immunomodulatory and proangiogenic factors.In an in vivo model,Dopa-gel treatment accelerated wound closure,increased vascularization,and promoted a shift in macrophages from a proinflammatory M1 phenotype to a prohealing and anti-inflammatory M2 phenotype within the wound area.Mechanistically,the focal adhesion kinase(FAK)/extracellular signal-related kinase(ERK)signaling pathway may mediate the promotion of skin defect healing by increasing paracrine secretion via the Dopa-gel.Additionally,proangiogenic factors can be induced through Rho-associated kinase-2(ROCK-2)/vascular endothelial growth factor(VEGF)-mediated paracrine secretion under tensile stress conditions.Taken together,these findings suggest that the multifunctional Dopa-gel,which has good mechanical properties similar to those of native skin tissue and enhanced immunomodulatory and angiogenic properties,is a promising scaffold for skin tissue regeneration.

Effect of Polyvinyl Alcohol in Inner Aqueous Phase on Stability of Millimeter-scale Capsules

The millimeter-scale capsules with controllable morphology,ultra-low permeability and excellent mechanical stability were fabricated by millifluidics.Viscosity of inner phase was adjusted to control the morphology and properties of the capsules.In detail,as the concentration of polyvinyl alcohol(PVA)increased from 0 to 8% in the inner phase of the capsules,the diameter of capsules decreased from 3.33 ± 0.01mm to 2.97 ± 0.01 mm,the shell thickness of capsules decreased from 0.183 ± 0.004 mm to 0.155 ± 0.003 mm.While the capsules had round shape and high sphericity.Notably,the capsules with 2% PVA in the inner phase had remarkably decreased water permeability and good morphological stability.Specifically,the end-time of water losing of the capsules was up to 49 days,while the dehydrated capsules maintained spherical appearance,and crushing force of the capsules was up to 13.73 ± 0.79 N,which ensured stability during processing and transportation.This research provides a new strategy for stable encapsulation of small molecules.

Electrospun polyvinyl alcohol fibres incorporating an antimicrobial gel for enzymatically controlled reactive oxygen species release

Wounds pose a risk to the skin,our body's primary defence against infections.The rise of antibiotic resistance has prompted the development of novel therapies.RO-101^(■)is an antimicrobial gel that delivers therapeutic levels of hydrogen peroxide(H_(2)O_(2)),a reactive oxygen species,directly to the wound bed.In this study,electrospinning was used to incorporate RO-101^(■)into a polyvinyl alcohol(PVA)sub-micron fibrous mesh that can act as a delivery agent,achieve a sustained release profile,and provide a barrier against infection.Adequate incorporation of this gel into sub-micron fibres was confirmed via nuclear magnetic resonance spectroscopy.Furthermore,scanning electron microscopy exhibited smooth and uniform meshes with diameters in the 200-500 nm range.PVA/RO-101 electrospun meshes generated H_(2)O_(2) in concentrations exceeding 1 m M/(g·m L)(1 m M=1 mmol/L)after 24 h,and the role of sterilisation on H_(2)O_(2) release was evaluated.PVA/RO-101meshes exhibited antimicrobial activity against both Gram-positive Staphylococcus aureus(S.aureus)and Gram-negative Pseudomonas aeruginosa(P.aeruginosa)bacteria,achieving viable count reductions of up to 1 log unit CFU/mm^(2)(CFU:colony-forming units).Moreover,these meshes were capable of disrupting biofilm formation,even against multidrug-resistant organisms such as methicillin-resistant S.aureus(MRSA).Furthermore,increasing the RO-101^(■)concentration resulted in higher H_(2)O_(2) production and an enhanced antimicrobial effect,while fibroblast cell viability and proliferation tests showed a concentration-dependent response with high cytocompatibility at low RO-101^(■)concentrations.This study therefore demonstrates the potential of highly absorbent PVA/RO-101 meshes as potential antimicrobial wound dressings.

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.

Preparation for Polyvinyl Alcohol Hollow Microsphere and Its Sustained Release Effect on Urea

[Objective] The aim of this study was to discuss the optimizing preparation conditions of polyvinyl alcohol(PVA)hollow microsphere and its application in the production of slow-release urea fertilizer.[Method]PVA hollow microsphere was prepared by the emulsion chemical cross-linking method,while its composition,morphology and particle size was analyzed by technologies of FT-IR,SEM and TEM respectively.Thus,factors such as rate of emulsified speed,crosslink temperature and linking agent amount with effects on morphology and particle size of hollow microsphere were also discussed in this study.Furthermore,based on the optimizing preparation conditions,PVA fertilizer carrier microsphere was prepared by coating urea to investigate its sustained release effect on urea.[Result]The optimizing preparation conditions of polyvinyl alcohol(PVA)hollow microsphere were as follows:rate of emulsified speed 6 000 r/min,crosslink temperature 35 ℃ and linking agent amount 25 ml.PVA fertilizer carrier microsphere had significant sustained release effect on urea,and the optimal cross-linking time was 3 hours.[Conclusion]This study provides theoretical basis for the development of new slow-release fertilizer.

阿仑膦酸钠/壳聚糖/聚乙烯醇复合水凝胶膜的制备与表征

背景:骨质疏松症是牙种植治疗的高风险因素,制备缓释阿仑膦酸钠的组织工程支架应用于骨质疏松患者口腔种植手术是当前口腔骨组织工程研究热点。目的:制备阿仑膦酸钠/壳聚糖/聚乙烯醇复合水凝胶膜,表征其缓释性能。方法:(1)采用物理交联法制备不同质量比(壳聚糖与聚乙烯醇的质量比分别为3∶7、5∶5、7∶3)的壳聚糖/聚乙烯醇复合水凝胶膜与单纯的壳聚糖、聚乙烯醇水凝胶膜,通过表征水凝胶膜的形貌、水接触角、力学性能、溶胀率与细胞相容性筛选适宜的水凝胶膜作为阿仑膦酸钠的载体。(2)制备含0,0.4,1.2,2.0 mg/L阿仑膦酸钠的单纯壳聚糖/聚乙烯醇复合水凝胶膜,将大鼠骨髓间充质干细胞分别与4组水凝胶膜共培养,通过CCK-8法与CD44免疫荧光染色检测水凝胶膜的细胞相容性。将载药壳聚糖/聚乙烯醇复合水凝胶膜浸泡于PBS中,采用紫外可见分光光度法检测复合水凝胶膜的药物释放性能。结果与结论:(1)表征结果显示,随着水凝胶膜中聚乙烯醇质量的增加,水凝胶膜的结构密度增加、孔隙率减少,水接触角(均在90°以内)、断裂伸长率与抗压强度增大,平衡溶胀率降低,对大鼠骨髓间充质干细胞的增殖均无影响,单纯壳聚糖水凝胶膜可促进大鼠骨髓间充质干细胞的黏附,3∶7、5∶5比例复合水凝胶膜不影响大鼠骨髓间充质干细胞的黏附,单纯聚乙烯醇水凝胶膜、7∶3比例复合水凝胶膜抑制大鼠骨髓间充质干细胞的黏附,综合以上结果,选择5∶5复合水凝胶膜作为阿仑膦酸钠的载体。(2)CCK-8检测结果显示,含0.4,1.2 mg/L阿仑膦酸钠组复合水凝胶膜无细胞毒性;CD44免疫荧光染色结果显示,含0.4 mg/L阿仑膦酸钠组复合水凝胶膜不影响大鼠骨髓间充质干细胞的黏附,含1.2,2.0 mg/L阿仑膦酸钠组复合水凝胶膜抑制大鼠骨髓间充质干细胞的黏附;含0.4,1.2,2.0 mg/L阿仑膦酸钠的壳聚糖/聚乙烯醇复合水凝胶膜在最初6 h内爆发性释放阿仑膦酸钠,此后均匀稳定地释放阿仑膦酸钠,释放时间达96 h以上。(3)结果表明,5∶5比例的壳聚糖/聚乙烯醇复合水凝胶膜具有良好的理化性能、细胞相容性,可以作为阿仑膦酸钠的缓释载体。

Immobilization of activated sludge using improved polyvinyl alcohol (PVA) gel

The microbial immobilization method using polyvinyl alcohol （PVA） gel as an immobilizing material was improved and used for entrapment of activated sludge. The oxygen uptake rate （OUR） was used to characterize the biological activity of immobilized activated sludge. Three kinds of PVA-immobilized particles of activated sludge, that is, PVA-boric acid beads, PVA-sodium nitrate beads and PVA-orthophosphate beads were prepared, and their biological activity was compared by measuring the OUR value. The bioactivity of both autotrophic and heterotrophic microorganisms of activated sludge was determined using different synthetic wastewater media （containing 250 mg/L COD and 25 mg/L NH4^＋ -N）. The experimental results showed that the bioactivity and stability of the three kinds of immobilized activated sludge was greatly improved after activation. With respect of the bioactivity and the mechanical stability, the PVA-orthophosphate method may be a promising and economical technique for microbial immobilization.

Hydrogen generation from polyvinyl alcohol-contaminated wastewater by a process of supercritical water gasification

Gasification of polyvinyl alcohol （PVA）-contaminated wastewater in supercritical water （SCW） was investigated in a continuous flow reactor at 723-873 K, 20-36 MPa and residence time of 20-450 s. The gas and liquid products were analyzed by GC/TCD, and TOC analyzer. The main gas products were H2, CH4, CO and CO2. Pressure change had no significant influence on gasification efficiency. Higher temperature and longer residence time enhanced gasification efficiency, and lower temperature favored the production of H2. The effects of KOH catalyst on gas product composition were studied, and gasification efficiency were analyzed. The TOC removal efficiency （RTOC）, carbon gasification ratio （RCG） and hydrogen gasification ratio （RHG） were up to 96.00%, 95.92% and 126.40% at 873 K and 60 s, respectively, which suggests PVA can be completely gasified in SCW. The results indicate supercritical water gasification for hydrogen generation is a promising process for the treatment ofPVA wastewater.

Fabrication and Characterization of One Interpenetrating Network Hydrogel Based on Sodium Alginate and Polyvinyl Alcohol

One interpenetrating network hydrogel based on sodium alginate (SA) and polyvinyl alcohol (PVA) was synthesized by combining the raw materials of PVA and SA with the double physical crosslinking methods of freezing thawing and Ca2+ crosslinking. The PVA-SA composite hydrogel have been characterized by scanning electron microscopy for surface morphology, infrared spectroscopy for investigating the chemical interactions between PVA and SA, X-ray diffraction for studying the PVA-SA composite structure property and thermal gravimetric for understanding the PVA-SA composite thermal stability. The swelling behavior and the degradation rate of the PVA-SA composite hydrogel were studied in simulated gastrointestinal fluid. Using bovine serum albumin (BSA) and salicylic acid as the model drugs, the release behavior of the PVASA composite hydrogel on macromolecular protein drugs and small molecule drug were evaluated. The results showed that the water absorption and degradation ability of the PVA-SA composite hydrogel was much better compared to the pure SA hydrogel or pure PVA hydrogel. The hydrogel exhibited remarkable pH sensitivity and the network was stable in the simulated intestinal fluid for more than 24 h. With the advantages such as mild preparation conditions, simple method, less reagent and none severe reaction, the PVA-SA composite hydrogel is expected to be a new prosperous facile sustained drug delivery carrier.

Preparation and Properties of Chitosan/Polyvinyl Alcohol Blended Fiber Membrane for Medical Dressing

The antibacterial dressing prepared by the electrospinning can play a role in protecting the wound,preventing infection and promoting wound healing,and have broad application prospects.Chitosan(CS)/polyvinyl alcohol(PVA)blended fiber membrane was successfully prepared by electrospinning.The fiber morphology,thermal properties and material composition of CS/PVA blended fiber membrane were studied,and the interaction between CS and PVA was analyzed,and the optimum blend ratio was also determined.Then glutaraldehyde(GA)steam cross-linking of the blended fiber membrane was carried out in order to improve the water resistance of the fiber membrane.At the same time,the effect of different cross-linking time on the water resistance of fiber membrane was investigated.The apparent morphology of the fiber membrane was observed by a scanning electron microscope(SEM).The results showed that with the increase of spinning solution concentration,the morphology of the fiber became more and more regular,and the fiber diameter increased gradually.The intermolecular interaction between CS and PVA was found by Fourier transform infrared(FTIR)spectroscopy and thermal properties,which improved the spinnability of CS electrospinning.After cross-linking,the water resistance of the fiber membrane was greatly improved,among which the effect of 4 h cross-linking was the best,and the water resistance of the fiber membrane increased by 64.89%.

Study on photodegradation of Azo dye by polyoxometalates/polyvinyl alcohol

A series of photocatalysts, K11[Ln(PW11O39)2]/PVA (Ln=La, Ce, Pr, Nd, Sm) were prepared by K11[Ln(PW11O39)2] (Ln=La, Ce, Pr, Nd, Sm) containing five kinds of lanthanides and polyvinyl alcohol as the support. The catalysts obtained were characterized by Fourier transform infrared spectra, UV-vis spectra, powder X-ray diffraction, and scanning electron microscopy, indicating that the structure of K11[Ln(PW11O39)2] and polyvinyl alcohol remained intact, respectively. The photocatalysts exhibited efficient catalytic activity to degrade methyl orange, Congo Red, Ponceau 2R. The maximal degradation conversions of the three kinds of dyes were 99.58%, 47.61%, 72.42%, respectively.

The Influence of Additives on Crystallization of Polyvinyl Chloride

Acetanilide, adipic acid and potassium hydrogen phthalate were chosen as nucleating agents of polyvinyl chloride（PVC）, and their effects on PVC crystallization were studied by differential scanning calorimetry, wide angle X-ray diffraction and fourier transform infrared spectroscopy. The experimental results indicate that all of the three additives are compatible with PVC to some extent, but adipic acid＇s compatibility with PVC is less satisfactory. The three additives can improve PVC crystallinity, and acetanilide can decrease PVC glass transition temperature（T）and narrow PVC melting range, while adipic acid and potassium hydrogen phthalate rise T of PVC and widen its melting range. All additives do not affect PVC crystal system and all g samples are in orthorhombic system. All additives can improve （200）, （110）, （210） and （201, 111） planes growing. Moreover, acetanilide and adipic acid can shrink PVC spacings and improve the crystal perfection of PVC, but potassium hydrogen phthalate swells spacings and reduces the perfection of PVC crystal.

SYNTHESIS，PROPERTY AND HEAT STABILITY FO RPOLYVINYLCHLORIDSOFANTIMONYTRIS（MERCAPTOACIDESTER）

Antimony mercaplde heat stabilizer for polyvinyl chlorideis synthesized from antimony trioxide and mercaptocarboxylic acid esters, HS(CH2).COoi-C8H17 (n=1～2) at 100～115 C In the presence of 0. 5%～1 % an organic acid catalyst. Some physicochemicalconstants of the compounds, such as density and refractive index, aredetermined. The complexes are hydrolabll in aqueous solutions andthe bond of Sb-S is weaker than that of Sb-o. The forming bondproperty of antimony tris (mercaptoacid ester ) has been elucidatedby measurement of infrared spectra in comparison with mercaptocarboxylic acid esters. The polyvinyl chloride resins containing antimony mercaptide heat stabilizers, do not darken at elevated temperatures and exhibit a high degree of stability. It is proposed that mercaptocarboxylic acid ester freeradicals can esterify PVC microradicals at carbon atoms with upaired electrons.

Electrically induced gel-sol transition of polyvinyl alcohol/polyacrylamide semi-interpenetrated hydrogels

Polyvinyl alcohol/polyacrylamide semi-interpenetrated hydrogels were prepared via freeze-thaw process. When a 20 V of DC was applied across the gels, the gels with lower polyacrylamide content underwent a contraction or partly turned into solution, while for the gels. with higher polyacrylamide concentration, a complete gel-sol transition was observed in a short time.

Fracture and Tensile Properties of Polyvinyl Alcohol Fiber Reinforced Cementitous Composites

Experiments were carried out to design polyvinyl alcohol （PVA） fiber reinforced cementitous composites （PVA-FRCCs） holding high ductility and energy consumption ability. Besides, the properties of each ingredients in composites, mixing method and technology for fresh mixture were described in detail. Then, the pseudo-strain-hardening （PSH） behavior was investigated in uniaxial tension test. As a result, the maximum ultimate tensile strain can reach 0.7 percent. On the other hand, the single edge notch （SEN） thin sheet specimens were employed to gain the normal tensile load via crack mouth opening displacement （CMOD） curves, which can show obvious PSH behavior. In addition, the curves can be divided into four zones whose fracture toughness calculation methods were discussed. The wedge splitting （WS） test method can be applied to discuss the fracture toughness. Moreover, fracture energy of SEN and WS specimens were both approximately evaluated.

Starch-g-poly (vinyl alcohol) as Compatibilizer for Reducing the Phase Separation Rates of Polyvinyl Alcohol/Cornstarch Pastes

Starch- g-poly(vinyl alcohol) as a compatibilizing agent for reducing the phase separation rates of polyvinyl alcohol/starch pastes has been investigated by blending and dissolving the two polymers in distilled water. The separation rates were quantitatively evaluated by the term of initiul demixing time. The grafted starches, with a series of grafting ratios, were prepared by grafting a number of vinyl acetate onto granular cornstarch in aqueous dispersion and then alcoholating in methanol. It was found that the addition of small amounts of starch- g poly (vinyl alcohol ) in the size compositions can effectively decrease the separation rates of the blended pastes in comparison to pure starch/PVA ones.Moreover, the influence of the grafting ratio, starch content, and PVA variety on the separation rates was also studied.

Cellulose Stabilized Polyvinyl Acetate Emulsion: Review

The global energy crisis and overconsumption of non-renewable resources have depleted natural resources, climatic changes with global warming, and rise in sea level. The research on alternate sources and chemicals has resulted in the usage of green materials. These biomaterials are sustainable sources, biodegradable, and are abundant in nature. The replacement of petrochemicals with biopolymers has gained much importance in this aspect. Conventionally, polyvinyl alcohol is employed as a protective colloid in polyvinyl acetate adhesive. Polyvinyl alcohol has the limitation of petroleum origin, is replaced by biopolymers. Starch being a biopolymer, has gained interest in replacing polyvinyl alcohol as a stabilizer. Cellulose has a low cost, and the most abundant biomaterial finds application as a reinforcing agent in conventional adhesives. Exploring cellulose as a stabilizer for polyvinyl acetate emulsion polymerization with reinforcement has created potential applicability of cellulose in adhesives. Surface hydroxyl groups in cellulose act as sites for functionalization, making it material for the adhesive sector. This review paper aims to showcase biomaterials, namely starch, and cellulose, in the adhesive field. A detailed review of cellulose as functional filler for polyvinyl acetate emulsion adhesives has been explained.

State of Research and Trends in the Development of Polyvinyl Acetate-Based Wood Adhesive

Synthetic wood adhesives, consisting of urea-formaldehyde resins (UF), phenol-formaldehyde resins (PF), melamine-formaldehyde resins (MF), and polyurethane resins, are widely used. For UF and MF, most investigations are concerned with reducing free formaldehyde content;for PF, most studies focused on finding new alternative chemicals to replace phenol. These adhesives come under the Carcinogenic, Mutagenic, and Reprotoxic chemicals (CMR) category. Due to global energy issues and dependency on petroleum sources, the focus has shifted to look for alternative and renewable raw material sources for wood adhesives. Conventionally available wood adhesives are polyvinyl alcohol (PVA) stabilized, with drawbacks like poor water resistance, poor heat resistance, low-temperature workability, and it’s based on petroleum resources. Polyvinyl acetate (PVAc) is non-resistant to moisture polymer, and if such adhesive joints are exploited in a moist environment, its strength substantially decreases. Sufficiently moisture-resistant adhesive joints are obtained by modifying PVAc dispersion with special compounds like reactive comonomer, Silanes, and modified PVA. To improve the workability at low temperature, Vinyl acetate (VAc) is copolymerized with specific comonomers like butyl acetate without affecting the performance properties. Here, we aim to present an overview of the research trend of PVAc-based adhesives in the wood industry. The review summarizes the current state of research PVAc-based adhesives.

Effect of Low-Pressure Nitrogen DC Plasma Treatment on the Surface Properties of Biaxially Oriented Polypropylene, Poly (Methyl Methacrylate) and Polyvinyl Chloride Films

In this study, commercial biaxially oriented polypropylene （BOPP）, polyvinyl chlo- ride （PVC） and poly （methyl methacrylate） （PMMA） films were treated with nitrogen plasma over different exposure times in a Pyrex tube surrounded by a DC variable magnetic field. The chemi- cal changes that appeared on the surface of the samples were investigated using Fourier transform infrared （FT4R） spectroscopy and attenuated total reflectance Fourier transform infrared （ATR- FTIR） spectroscopy after treatment for 2 min, 4 min and 6 rain in a nitrogen plasma chamber. Effects of the plasma treatment on the surface topographies and contact angles of the untreated and plasma treated films were also analyzed by atomic force microscopy （AFM） and a contact angle measuring system. The results show that the plasma treated films become more hydrophilic with an enhanced wettability due to the formation of some new polar groups on the surface of the treated films. Moreover, at higher exposure times, the total surface energy in all treated films increased while a reduction in contact angle occurred. The behavior of surface roughness in each sample was completely different at higher exposure times.

Preparation of felt-metal supported modified polyvinyl alcohol composite hydrophilic ultrafiltration membrane

A novel technology of preparation of felt-metal supported modified polyvinyl alcohol（PVA） ultrafiltration（UF） membrane was invented, which could avoid the blockage of the holes of support layer and the leakage of the casting solution through the holes of support layer. Felt-metal supported ferric sulfate modified PVA composite UF membranes were prepared by the innovative technology. The results show that the composite membranes are used to treat 1 000 mg/L oil/water emulsion at trans-membrane pressure from 0.25 to 0.45 MPa, the permeate flux is from 36 to 52 L/（m2·h）, and the retention of chemical oxygen demand（COD） is over 92%. The composite membrane resistance increases with the increase of trans-naembrane pressure.