Synthesis of poly(vinyl benzal) from poly(vinyl alcohol) in nonaqueous medium

Poly(vinyl alcohol) (PVA) is soluble only in water and so some important derivatives like esters cannot be prepared from PVA. The 100% conversion of PVA to acetal is also elusive as there is strong intermolecular and intramolecular hydrogen bonding. However, PVA can be dissolved in a nonaqueous medium in the presence of a small amount of C₂H₅NO₃ · DMSO(EN · DMSO) and so a maximum extent of conversion may be possible. Here, we report the preparation of poly(vinyl benzal) (PVB) by acid-catalyzed homogeneous acetalization of PVA with benzaldehyde in a nonaqueous medium. The formation of PVB was confirmed by IR and ¹H-NMR spectra. The molecular mass of the polymer was determined by the GPC method. The PVB prepared had a degree of acetalization of 95 mol%. The glass transition temperature, T_g was measured from differential scanning calorimetric (DSC) thermograms. Thermal stabilities were checked by thermogravimetric analysis (TGA) and differential thermogravimetry (DTG). A possible mechanism of three-step thermal decomposition of PVB is proposed. © 1996 John Wiley & Sons, Inc.     

Synthesis of poly(vinyl butyral)s in homogeneous phase and their thermal properties

The condensation reaction of butyraldehyde (BA) with poly(vinyl alcohol) (PVA) to give poly(vinyl butyral) (PVB) was studied in detail using N‐methyl‐2‐pyrrolidone (NMP) as solvent for PVA and PVBs. PVBs having various degrees of acetalization were obtained. The acetalization reaction under a variety of conditions gave at best a polymer with 97% acetalization. The extent of modification and the structure of the polymer, i.e., the ratio of acetal units from meso and racemic dyads of PVA, were determined by ¹H‐NMR. The acetalization degree was reflected in the solubility of PVB; all products were soluble in NMP. PVBs were characterized by IR spectroscopy and ¹H and ¹³C‐NMR. The glass transition temperatures of PVBs, determined by DSC, increased as vinyl alcohol units increased and displayed a positive departure from linearity. Thermal degradation of PVBs was studied using differential thermal analysis (DTA) and thermogravimetry (TGA) under dynamic conditions in nitrogen. The content of hydroxyl groups had an effect on the thermal stability of PVBs; the thermal stability of PVBs decreased as vinyl alcohol units increased. The apparent activation energy of the decomposition was determined by the Kissinger and Flynn–Wall methods, which agree well. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5007–5017, 2006     

Synthesis of poly(vinyl propionate) from poly(vinyl alcohol) in nonaqueous medium using ethyl nitrate dimethyl sulfoxide as a catalyst

Poly(vinyl alcohol) (PVA) can be dissolved in a nonaqueous medium in the presence of catalytic concentration of ethyl nitrate dimethyl sulfoxide, C₂H₅ONO₂·DMSO. From the PVA solution, poly(vinyl propionate), PVPR was prepared by the homogeneous esterification of PVA with propionic acid. The ester thus formed contained some unconverted hydroxyl group. The formation of the ester was confirmed by the IR and ¹H‐NMR spectra. The molecular weight of the ester was determined by GPC and intrinsic viscosity (η) was determined by viscometric method. Glass transition temperature, T_g, was obtained from differential scanning calorimetric (DSC) analysis. Thermal stabilities of the ester were checked by thermogravimetric analysis (TGA) and differential thermogravimetric (DTG) analysis. The efficiency of the ester as a flow improver of crude oil was also examined. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5675–5679, 2006     

Novel network polymer electrolytes containing fluorine and sulfonic acid lithium prepared by ultraviolet polymerization

Poly(vinyl alcohol) (PVAL) and vinyl acetate‐vinyl alcohol copolymers (VAVAL) were esterified with 3,5‐dinitrobenzoyl chloride using the cycled urea N,N′‐dimethylpropyleneurea (1,3‐dimethyl‐3,4,5,6‐tetrahydro‐2(1H)‐pyrimidinone) (DMPU) as the solvent. Vinyl alcohol‐vinyl‐3,5‐dinitrobenzoate copolymers (VALVDNB) and vinyl acetate‐vinyl‐3,5‐dinitrobenzoate copolymers (VAVDNB) were obtained. High degrees of esterification were obtained when PVAL was esterified (86%). The degree of transformation was determined by ¹H‐NMR as well as by chemical analysis, and the structure of the resulting polymers by means of IR spectroscopy and ¹H‐ and ¹³C‐NMR. The microstructure of PVA, PVAL, VAVAL copolymers and VALVDNB copolymers were determined from ¹H‐ and ¹³C‐NMR techniques. The sequence distributions for VAVAL copolymers prepared by base‐catalyzed transesterification of PVA were blocky, while the distributions were close to random for VALVDNB copolymers obtained by esterification of PVAL. Thermal properties were studied by DSC. The T_g values of VAVAL, VALVDNB, and VAVDNB copolymers as a function of copolymer compositions were determined. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Miscibility and phase structure of binary blends of poly(L‐lactide) and poly(vinyl alcohol)

Blend films of poly(L ‐lactide) (PLLA) and poly(vinyl alcohol) (PVA) were obtained by evaporation of hexafluoroisopropanol solutions of both components. The component interaction, crystallization behavior, and miscibility of these blends were studied by solid‐state NMR and other conventional methods, such as Fourier transform infrared (FTIR) spectra, differential scanning calorimetry (DSC), and wide‐angle X‐ray diffraction (WAXD). The existence of two series of isolated and constant glass‐transition temperatures (T_g's) independent of the blend composition indicates that PLLA and PVA are immiscible in the amorphous region. However, the DSC data still demonstrates that some degree of compatibility related to blend composition exists in both PLLA/atactic‐PVA (a‐PVA) and PLLA/syndiotactic‐PVA (s‐PVA) blend systems. Furthermore, the formation of interpolymer hydrogen bonding in the amorphous region, which is regarded as the driving force leading to some degree of component compatibility in these immiscible systems, is confirmed by FTIR and further analyzed by ¹³C solid‐state NMR analyses, especially for the blends with low PLLA contents. Although the crystallization kinetics of one component (especially PVA) were affected by another component, WAXD measurement shows that these blends still possess two isolated crystalline PLLA and PVA phases other than the so‐called cocrystalline phase. ¹³C solid‐state NMR analysis excludes the interpolymer hydrogen bonding in the crystalline region. The mechanical properties (tensile strength and elongation at break) of blend films are consistent with the immiscible but somewhat compatible nature of these blends. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 762–772, 2001     

Water-soluble temperature-responsive poly(vinyl alcohol-co-vinyl acetal)s

Summary In order to obtain novel temperature-responsive copolymers, poly(vinyl alcohol) (PVA) was chemically modified by introducing cyclic acetal functionalities in the polymer chain. The acetalization reaction was carried out with acetaldehyde in water The degree of acetalization was controlled in the range 10–25% by the initial aldehyde concentration. The copolymers obtained were characterized by 1D (¹H, ¹³C, DEPT) and 2D (COSY) NMR techniques as well as by viscometry. The thermo-responsive properties were evaluated by measuring the cloud point temperature (T_cp) of the aqueous copolymer solutions.     

Preparation of high molecular weight poly(vinyl alcohol) with high yield using low‐temperature solution polymerization of vinyl acetate

Vinyl acetate (VAc) was solution‐polymerized in tertiary butyl alcohol (TBA) and in dimethyl sulfoxide (DMSO) having low chain transfer constant at 30, 40, and 50°C, using a low temperature initiator, 2,2′‐azobis(2,4‐dimethylvaleronitrile) (ADMVN). The effects of polymerization temperature and initiator concentration were investigated in terms of polymerization behavior and molecular structures of poly(vinyl acetate) (PVAc) and corresponding poly(vinyl alcohol) (PVA) obtained by saponification with sodium hydroxide. The polymerization rates of VAc in TBA and in DMSO were proportional to the 0.49 and 0.72 powers of ADMVN concentration, respectively. For the same polymerization conditions, TBA was absolutely superior to DMSO in increasing the molecular weight of PVA. In contrast, TBA was inferior to DMSO in causing conversion to polymer, indicating that the initiation rate of VAc in TBA was lower than that in DMSO. These effects could be explained by a kinetic order of ADMVN concentration calculated using initial rate method and by an activation energy difference of polymerization obtained from the Arrhenius plot. Low‐temperature solution polymerization of VAc in TBA or DMSO by adopting ADMVN proved successful in obtaining PVA of high molecular weight (number–average degree of polymerization (P_n): 4100–6100) and of high yield (ultimate conversion of VAc into PVAc: 55–80%) with diminishing heat generated during polymerization. In the case of bulk polymerization of VAc at the same conditions, maximum P_n and conversion of 5200–6200 and 20–30% was obtained, respectively. The P_n and lightness were higher, and the degree of branching was lower with PVA prepared from PVAc polymerized at lower temperatures in TBA. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1003–1012, 2001     

Synthesis,characterization, and drug release activity of structurally modified poly(vinyl alcohol)

The main aim of the present investigation is synthesis of drug‐grafted poly(vinyl alcohol) (PVA) for sustainable drug release in order to avoid bulk release and unwanted side effects. Here, the PVA was structurally modified with five different drug molecules in DMSO medium at 85 °C under N₂ atmosphere for 2 h. The structure of modified PVA was confirmed by FTIR and ¹H NMR spectra and further it was characterized by TGA, DSC, and SEM. The tensile strength and % elongation for the structurally modified PVA were determined. The FTIR spectrum showed peaks corresponding to the C?O and C? S stretching due to the grafted drug molecules. The ¹H NMR spectrum showed the acrylic CH₂ proton signal of PVA around 1.6 ppm. The SEM showed different surface morphology for the structurally modified PVA. The mechanical properties of the structurally modified PVA was found to be reduced due to the presence of traces of solvent molecules and the breaking of inter‐ and intramolecular hydrogen bonding. The sustainable drug release through hydrolysis mechanism was tested at the pH of 7.3. Generally, the drug release followed the Korsmeyer–Peppas model with Fickian drug transportation mechanism except Furosemide (Fur)‐grafted PVA system at the pH of 7.3. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46620.     

Development of a nonaqueous solvent system for poly(vinyl alcohol) and its characterization

Solubility of poly(vinyl alcohol) (PVA) in water prevents the preparation of various derivatives through homogeneous techniques as most of the derivatives thus formed are insoluble in aqueous medium. There are a number of solvents that can swell PVA under hot conditions but cannot dissolve PVA. In the present study, N,N‐dimethyl acetamide (DMAc) has been identified as solvent in which PVA can be dissolved in the presence of an equimolar amount of lithium chloride (LiCl). ¹H nuclear magnetic resonance (¹H‐NMR), ¹³C‐NMR, infrared (IR), and X‐ray diffraction (XRD) studies have been carried out to characterize the regenerated poly(vinyl alcohol) (RPVA). DMAc–LiCl is found to be a true solvent system for dissolution of PVA. An attempt has also been made to prepare poly(vinyl acetate) from this solution of PVA by a homogeneous technique. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 663–669, 1999     

Characterization of strong polyelectrolyte hydrogels based on poly(vinyl alcohol)

Maleic anhydride (MA) was grafted onto both partially and fully hydrolyzed poly(vinyl alcohol) (PVA) in the presence of an initiator. Strong polyelectrolyte polymers were prepared by sulfonation of PVA–MA grafts. The sulfonation was completed by reaction of hydroxyl groups of PVA–MA grafts with two different sulfonating reagents (chlorosulfonic acid and pyridine sulfonic acid). The sulfonation degree was evaluated by acid–base titration and ¹H NMR analysis. The solution behaviour of the prepared grafts was evaluated from viscosity measurements. Four kinds of water‐insoluble PVA–MA and PVA–MA‐SO₃H hydrogels were prepared by heat treatment, physical gelation and chemical crosslinking with different weight ratios of N,N‐methylene bisacrylamide (MBA) crosslinker. The swelling parameters were measured for all prepared gels in deionized water and aqueous solutions at different pH values from 2 to 12 having constant ionic strength (I = 0.1). All gels exhibit a different swelling behaviour upon environmental pH changes. Copyright © 2004 Society of Chemical Industry     

Rheological properties of high molecular weight (HMW) syndiotactic poly(vinyl alcohol) (PVA)/HMW atactic PVA blend solutions

To identify the effect of blend ratios of syndiotacticity‐rich poly(vinyl alcohol) (s‐PVA)/atactic PVA (a‐PVA) having similar number‐average degrees of polymerization (P_n)s of 4000 and degrees of saponification (DS)s of 99.9% on the rheological properties of s‐PVA/a‐PVA/water solutions, water‐soluble s‐PVA and a‐PVA with different syndiotactic diad contents of 58.5 and 54.0%, respectively, were prepared by bulk copolymerization of vinyl pivalate and vinyl acetate (VAc) and solution polymerization of VAc, followed by saponifying the corresponding copoly(vinyl pivalate/vinyl acetate) and poly(vinyl acetate). The blend ratios played a significant role in rheological behavior. Over the frequency range of 10^?1–10² rad/s, s‐PVA/a‐PVA blend solutions with larger s‐PVA content show more shear thinning at similar (P_n)s and (DS)s of polymer, suggesting that PVA molecules are more readily oriented as s‐PVA content increases. Yield stress is higher for s‐PVA/a‐PVA blend solutions with larger s‐PVA content at similar (P_n)s and (DS)s of polymer. This indicates that more domains with internal order are produced at larger s‐PVA content in s‐PVA/a‐PVA blend solutions. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3934–3939, 2006     

Melt processing of poly(vinyl alcohol) through adding magnesium chloride hexahydrate and ethylene glycol as a complex plasticizer

The melt processing of poly(vinyl alcohol) (PVA) was achieved using magnesium chloride hexahydrate (MgCl₂·6H₂O) and ethylene glycol as a complex plasticizer. The interaction between the complex plasticizer and PVA was studied by Fourier transform infrared spectroscopy (FT‐IR). The PVA films were characterized using X‐ray diffraction (XRD), differential scanning calorimetry, thermogravimetric analysis (TGA), scanning electron microscope, and dynamic thermomechanical analysis (DMA) techniques. The band shift of the observed peak around 3335 cm^?1 in the FT‐IR spectra indicates that the complex plasticizer MgCl₂·6H₂O and ethylene glycol could form strong interactions with PVA and thus interrupt the intermolecular and intramolecular hydrogen bonding in PVA. The XRD results show that the addition of the complex plasticizer would significantly destroy the crystallites of PVA and result to the decrease of the degree of crystallinity of PVA. The melting point was reduced from 229°C of pure PVA to around 170°C after the plasticization. The TGA studies show that with the complex plasticizer, the thermal stability of PVA is improved. PVA plasticized by 30 wt% MgCl₂·6H₂O and 10 wt% ethylene glycol shows the tensile strength of 33 MPa and the elongation at break of 362%. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Preparation and swelling properties of semi‐IPN hydrogels based on chitosan‐g‐poly(acrylic acid) and phosphorylated polyvinyl alcohol

The phosphorylated poly(vinyl alcohol) (P‐PVA) samples with various substitution degrees were prepared through the esterification reaction of PVA and phosphoric acid. By using chitosan (CTS), acrylic acid (AA) and P‐PVA as raw materials, ammonium persulphate (APS) as an initiator and N,N‐methylenebisacrylamide as a crosslinker, the CTS‐g‐PAA/P‐PVA semi‐interpenetrated polymer network (IPN) ssuperabsorbent hydrogel was prepared in aqueous solution by the graft copolymerization of CTS and AA and followed by an interpenetrating and crosslinking of P‐PVA chains. The hydrogel was characterized by Fourier transform infrared (FTIR), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC) techniques, and the influence of reaction variables, such as the substitution degree and content of P‐PVA on water absorbency were also investigated. FTIR and DSC results confirmed that PAA had been grafted onto CTS backbone and revealed the existence of phase separation and the formation of semi‐IPN network structure. SEM observations indicate that the incorporation of P‐PVA induced highly porous structure, and P‐PVA was uniformly dispersed in the polymeric network. Swelling results showed that CTS‐g‐PAA/P‐PVA semi‐IPN superabsorbent hydrogel exhibited improved swelling capability (421 g·g^?1 in distilled water and 55 g·g^?1 in 0.9 wt % NaCl solution) and swelling rate compared with CTS‐g‐PAA/PVA hydrogel (301 g·g^?1 in distilled water and 47 g·g^?1 in 0.9 wt % NaCl solution) due to the phosphorylation of PVA. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effects of solvent adsorption on solution properties of poly(vinyl alcohol)/dimethylsulfoxide/water ternary systems

In this study, the solvent adsorption phenomena of poly(vinyl alcohol) (PVA) in cosolvent mixtures of dimethylsulfoxide (DMSO; solvent 1) and water (solvent 2) were investigated. Typically, this cosolvent mixture could form hydrogen‐bonded DMSO/(water)₂ complexes, involving one DMSO and two water molecules. Because of the complex formation in the cosolvent mixtures, PVA chains preferentially adsorb water molecules at DMSO mole fraction X₁ < 0.33, but preferentially adsorb DMSO molecules at X₁ > 0.33. The preferential adsorption of DMSO (a good solvent for PVA) could cause the relatively extended conformation of PVA chains in solutions because of the increase in excluded volume effect. Because of various interactions between PVA chains and cosolvent mixtures, the aggregation and gelation behaviors of PVA solutions were significantly affected by the composition of cosolvent mixture. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3211–3217, 2004     

Characterization of grafting in the emulsion polymerization of vinyl acetate using poly(vinyl alcohol) as stabilizer

Emulsion polymerizations of vinyl acetate (VAc) with polyvinyl alcohol (PVA) as emulsifier were carried out by both batch and semicontinuous processes. The extent of grafting of vinyl acetate onto the PVA chains was investigated by a new method for separating the various polymer fractions in high solids content latexes. The quantification was carried out by a three‐step separation and selective solubilization of the PVAc latexes. After the separation, the water‐soluble PVA and the solvent‐soluble PVAc components were characterized by gel permeation chromatography and ¹³C–NMR, from which the accuracy of this method was verified. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 1739–1747, 2001     

Preparation of ultrahigh molecular weight syndiotactic poly(vinyl alcohol) microfibrillar fibers by low‐temperature solution polymerization of vinyl pivalate in tertiary butyl alcohol and saponification

Vinyl pivalate (VPi) was solution polymerized in tertiary butyl alcohol (TBA) and in dimethyl sulfoxide (DMSO) with a low chain transfer constant using a low temperature initiator, 2,2′‐azobis(2,4‐ dimethylvaleronitrile) (ADMVN). The effects of polymerization temperature and initiator concentration were investigated in terms of polymerization behavior and molecular structures of poly(vinyl pivalate) (PVPi) and its saponification product poly(vinyl alcohol) (PVA). TBA was absolutely superior to DMSO in increasing the syndiotacticity and molecular weight of PVA. In contrast, TBA was inferior to DMSO in causing conversion to polymer, indicating that the initiation rate of VPi production in TBA was lower than that in DMSO. These effects could be explained by a kinetic order of ADMVN concentration, calculated by the initial rate method. Low‐temperature solution polymerization of VPi in TBA or DMSO by adopting ADMVN proved to be successful in obtaining PVA of ultrahigh molecular weight [maximum number‐average degree of polymerization (P_n): 13,500–17,000] and of high yield (ultimate conversion of VPi into PVPi: 55–83%). In the case of bulk polymerization of VPi at the same conditions, maximum P_n and conversion were 14,500–17,500 and 22–36%, respectively. The P_n and syndiotactic diad content were much higher and the degree of branching was lower with PVA prepared from PVPi polymerized at lower temperatures in TBA. Moreover, PVA from the TBA system was fibrous, with a high degree of orientation of the crystallites, indicating the syndiotactic nature of TBA polymerization. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 1992–2003, 2002     

ϵ‐caprolactone grafting on a poly(vinyl alcohol‐co‐vinyl acetate) in the melt without added initiator

Polycaprolactone (PCL) grafting on vinyl alcohol‐co‐vinyl acetate) (PVA‐Ac), was investigated in the melt at high temperature (170°C), below the PVA‐Ac melting point, by ring opening polymerization of ?‐caprolactone initiated by metal alkoxyde sites present in PVA‐Ac: no additional initiator was used. The obtained average structures were determined by ¹H NMR. As expected, small grafts, with low average polymerization degree (DP), were obtained, between 4 and 12 h of reaction. These DP are due to exchange reactions between hydroxyl groups and PCL growing chains. The PVA‐Ac was shown to be partially substituted by short PCL grafts. The DP linearly increased with the initial Lactone/PVA‐Ac ratio, and the substituted alcohol sites rate were limited to 63%.It was shown that the used reactive system is characterized by a quazi‐living polymerization mechanism. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Preparation of water‐swollen hydrogel membranes for gas separation

Water‐swollen hydrogel (WSH) membranes for gas separation were prepared by the dip‐coating of asymmetric porous polyetherimide (PEI) membrane supports with poly(vinyl alcohol) (PVA)–glutaraldehyde (GA), followed by the crosslinking of the active layer by a solution method. Crosslinked PVA/GA film of different blend compositions (PVA/GA = 1/0.04, 0.06, 0.08, 0.10, 0.12 mol %) were characterized by differential scanning calorimetry (DSC) and their water‐swelling ratio. The swelling behavior of PVA/GA films of different blend compositions was dependent on the crosslinking density and chemical functional groups created by the reaction between PVA and GA, such as the acetal group, ether linkage, and unreacted pendent aldehydes in PVA. The permeation performances of the membranes swollen by the water vapor contained in a feed gas were investigated. The behavior of gas permeation through a WSH membrane was parallel to the swelling behavior of the PVA/GA film in water. The permeation rate of carbon dioxide through the WSH membranes was 10⁵ (cm³ cm^?2 s^?1 cmHg) and a CO₂/N₂ separation factor was about 80 at room temperature. The effect of the additive (potassium bicarbonate, KHCO₃) and catalyst (sodium arsenite, NaASO₂) on the permeation of gases through these WSH membranes was also studied. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1785–1791, 2001     

Synthesis of poly(vinyl alcohol)‐graft‐poly(ε‐caprolactone) and poly(vinyl alcohol)‐graft‐poly(lactide) in melt with magnesium hydride as catalyst

Grafting of poly(ε‐caprolactone) (PCL) and poly(lactide) (PLA) chains on poly(vinyl alcohol) backbone (PVA degree of hydrolysis 99%) was investigated using MgH₂ environmental catalyst and melt‐grown ring‐opening polymerization (ROP) of ε‐caprolactone (CL) and L ‐lactide (LA), that avoiding undesirable toxic catalyst and solvent. The ability of MgH₂ as catalyst as well as yield of reaction were discussed according to various PVA/CL/MgH₂ and PVA/LA/MgH₂ ratio. PVA‐g‐PCL and PVA‐g‐PLA were characterized by ¹H‐ and ¹³C‐NMR, DSC, SEC, IR. For graft copolymers easily soluble in tetrahydrofuran (THF) or chloroform, wettability and surface energy of cast film varied in relation with the length and number of hydrophobic chains. Aqueous solution of micelle‐like particles was realized by dissolution in THF then addition of water. Critical micelle concentration (CMC) decreased with hydrophobic chains. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Original synthesis of polyvinyl butyral with a green deep eutectic solvent and a weakly polyacrylic acid from polyvinyl alcohol and the impacts of the chains structures of polyvinyl alcohol

In this work, an environmentally-friendly deep eutectic solvent (DES) was employed as a catalyst to generate polyvinyl butyral (PVB) resins from polyvinyl alcohol (PVA) with a weakly acidic polymer (polyacrylic acid [PAA]) as an emulsifier. Finally, high viscosity PVB resins with molecular weight of 110,000–200,000 g · mol⁻¹ and acetalization degree above 83% were successfully synthesized, which was found to satisfy the requirements for interlayer films between safety glass. Furthermore, it was well proved that the properties of PVB resins immensely depend on the molecular structures of the PVA. The molecular weight of the PVB, independent of alcoholic degrees of the PVA, indicated an upward trend with the increase of the molecular weight of the PVA. As for these four PVBs with high molecular weight, the T_g was sensitive to the content of hydroxyl and acetal groups rather than molecular weight, associated with the inter- or intra-molecule hydrogen bond between  OH. PVB-1799 and PVB-1797 had higher T_i and T_g than that of PVB-1788 and PVB-1795 because the former had low contents of vinyl acetate group (VAc) and alcohol hydroxyl group (VOH). The tensile strength of PVBs was all higher than 30 Mpa, and the elongation at break was about 300% due to their high molecular weights.