The advantages of using starch graft copolymers as warp sizes in textile were briefly discussed, and the factors of affecting adhesive capacity to the fiber were analysed. By using eerie ammonium nitrate as an initiat...The advantages of using starch graft copolymers as warp sizes in textile were briefly discussed, and the factors of affecting adhesive capacity to the fiber were analysed. By using eerie ammonium nitrate as an initiator under nitrogen atomosphere, a number of vinyl and/or acrylic monomers such as acrylic acid, acrylamide, methyl acrylate, ethyl acrylate, butyl acrylate, hydroxyethyl acrylate, methyl methacrylate, butyl methacrylate, vinyl acetate and the combinations among them were graft copolymerized respectively onto granular corn starch in aqueous dispersion. The adhesive capacity of these starch graft copolymers to polyester/cotton fibers was evaluated by a slightly sized rovings according to V. K. Aggarwal’s method which measures the breaking strength and elongation of the rovings impregnated with the size paste. The influences of the monomers and their combinations, the grafting technological processes and the pretreatment methods before graft copolymerization upon adhesive capacity have been展开更多
In this work, the surface properties of novel sugar-containing polymers, α-allyl glucoside (AG)/acrylonitrile (AN)copolymers, were studied by contact angle, protein adsorption and cell adhesion measurements. It was f...In this work, the surface properties of novel sugar-containing polymers, α-allyl glucoside (AG)/acrylonitrile (AN)copolymers, were studied by contact angle, protein adsorption and cell adhesion measurements. It was found that the contactangle of the copolymer films decreased from 68° to 30° with the increase of AG content in the copolymer. The adsorptionamount of bovine serum albumin (BSA) and the adhesive macrophage onto the film surface also decreased significantly withincreasing α-allyl glucoside content from 0 to 42 wt% in the copolymer. These preliminary results reveal that both thehydrophilicity and the biocompatibility of polyacrylonitrile-based membranes could be improved by copolymerizin gacrylonitrile with vinyl carbohydrates.展开更多
The design of crosslinking domains is a vital factor to create functional hydrogels with controlled physical,mechanical,and adhesive properties.This paper demonstrates versatile synthetic systems of micelle-crosslinke...The design of crosslinking domains is a vital factor to create functional hydrogels with controlled physical,mechanical,and adhesive properties.This paper demonstrates versatile synthetic systems of micelle-crosslinked hydrogels with highly stretchable,self-healing,and selectively adhesive properties.For this,methacrylate-bearing random copolymer micelles are designed as physical and covalent crosslink domains via the self-assembly of amphiphilic random copolymers carrying hydrophilic poly(ethylene glycol)(PEG),hydrophobic butyl or dodecyl groups,and methacrylate-terminal PEG in water.The size,aggregation number,and pendant methacrylate number of the micelles are controlled by the composition and degree of polymerization.Hydrogels are efficiently obtained from the free radical polymerization of hydrophilic monomers such as PEG acrylate and acrylamide in the presence of the micelle crosslinkers in water.Owing to the dynamic yet selective chain exchange properties of the micelle domains,the hydrogels are highly stretchable up to over 1000%and show self-healing and selectively adhesive properties.The self-healing of hydrogels is promoted upon heating due to the fast chain exchange of the micelle domains,whereas hydrogels consisting of micelles with different alkyl groups are never adhesive because of their self-sorting properties.展开更多
In this work, the membrane surface of poly（acrylonitrile-co-2-hydroxyethyl methacrylate） （PANCHEMA） was chemically modified by anchoring of phospholipid moieties. The process involved the reaction of hydroxyl grou...In this work, the membrane surface of poly（acrylonitrile-co-2-hydroxyethyl methacrylate） （PANCHEMA） was chemically modified by anchoring of phospholipid moieties. The process involved the reaction of hydroxyl groups on the membrane surface with 2-chloro-2-oxo-1,3,2-dioxaphospholane （COP） followed by the ring-opening reaction of COP with trimethylamine. Chemical differences between the original and the modified membranes were characterized by FT-IR and XPS, It was found that the amount of macrophage adhered on the modified membrane surface is substantially lower than that on polyacrylonitrile （PAN） and PANCHEMA membranes under the same condition, The morphological change of the adherent cell is also suppressed by the generation ofphospholipid moieties on the membrane surface.展开更多
To improve the hydrophilicity of polyacrylonitrile-based membranes, sugar moieties were incorporated into acrylonitrile-based copolymers via the radical copolymerization of α-allyl glucoside(AG) with acrylonitrile(AN...To improve the hydrophilicity of polyacrylonitrile-based membranes, sugar moieties were incorporated into acrylonitrile-based copolymers via the radical copolymerization of α-allyl glucoside(AG) with acrylonitrile(AN) with 2,2′-azobis-iso-butyronitrile(AIBN) as the initiator in dimethyl sulphoxide(DMSO). It was found that the yield increased with the increase of the initiator concentration and reaction time, while it decreased with the increase of the monomer molar ratio of AG to AN. Raising the AG proportion in the monomer mixture resulted in the increase of the AG content in the copolymer. M_v of the copolymers decreased with increasing the AG monomer fraction in feed. The copolymers were fabricated into dense membranes and their surface properties were studied by means of the water contact angle measurement and platelet adhesion tests. It was found that the static water contact angle on the membrane decreased significantly from 70° to 33° with the increase of the AG content. The adhesive number of platelets on the membrane surface also decreased significantly with increasing AG content in the copolymers. These results demonstrate that the hydrophilicity and biocompatibility of the acrylonitrile-based copolymer membranes could be improved efficiently by the copolymerization of acrylonitrile with vinyl carbohydrates.展开更多
文摘The advantages of using starch graft copolymers as warp sizes in textile were briefly discussed, and the factors of affecting adhesive capacity to the fiber were analysed. By using eerie ammonium nitrate as an initiator under nitrogen atomosphere, a number of vinyl and/or acrylic monomers such as acrylic acid, acrylamide, methyl acrylate, ethyl acrylate, butyl acrylate, hydroxyethyl acrylate, methyl methacrylate, butyl methacrylate, vinyl acetate and the combinations among them were graft copolymerized respectively onto granular corn starch in aqueous dispersion. The adhesive capacity of these starch graft copolymers to polyester/cotton fibers was evaluated by a slightly sized rovings according to V. K. Aggarwal’s method which measures the breaking strength and elongation of the rovings impregnated with the size paste. The influences of the monomers and their combinations, the grafting technological processes and the pretreatment methods before graft copolymerization upon adhesive capacity have been
基金The authors are grateful to the National Natural Science Foundation of China for financial support(Grant No.20074033).
文摘In this work, the surface properties of novel sugar-containing polymers, α-allyl glucoside (AG)/acrylonitrile (AN)copolymers, were studied by contact angle, protein adsorption and cell adhesion measurements. It was found that the contactangle of the copolymer films decreased from 68° to 30° with the increase of AG content in the copolymer. The adsorptionamount of bovine serum albumin (BSA) and the adhesive macrophage onto the film surface also decreased significantly withincreasing α-allyl glucoside content from 0 to 42 wt% in the copolymer. These preliminary results reveal that both thehydrophilicity and the biocompatibility of polyacrylonitrile-based membranes could be improved by copolymerizin gacrylonitrile with vinyl carbohydrates.
基金Japan Society for the Promotion of Science KAKENHI,Grant/Award Numbers:JP19K22218,JP20H02787,JP20H05219,JP22H04539The Ogasawara Foundation for the Promotion of Science&Engineering+1 种基金Noguchi InstituteIketani Science and Technology Foundation。
文摘The design of crosslinking domains is a vital factor to create functional hydrogels with controlled physical,mechanical,and adhesive properties.This paper demonstrates versatile synthetic systems of micelle-crosslinked hydrogels with highly stretchable,self-healing,and selectively adhesive properties.For this,methacrylate-bearing random copolymer micelles are designed as physical and covalent crosslink domains via the self-assembly of amphiphilic random copolymers carrying hydrophilic poly(ethylene glycol)(PEG),hydrophobic butyl or dodecyl groups,and methacrylate-terminal PEG in water.The size,aggregation number,and pendant methacrylate number of the micelles are controlled by the composition and degree of polymerization.Hydrogels are efficiently obtained from the free radical polymerization of hydrophilic monomers such as PEG acrylate and acrylamide in the presence of the micelle crosslinkers in water.Owing to the dynamic yet selective chain exchange properties of the micelle domains,the hydrogels are highly stretchable up to over 1000%and show self-healing and selectively adhesive properties.The self-healing of hydrogels is promoted upon heating due to the fast chain exchange of the micelle domains,whereas hydrogels consisting of micelles with different alkyl groups are never adhesive because of their self-sorting properties.
基金This work was financially supported by the National Natural Science Foundation of China(No.50273032).
文摘In this work, the membrane surface of poly（acrylonitrile-co-2-hydroxyethyl methacrylate） （PANCHEMA） was chemically modified by anchoring of phospholipid moieties. The process involved the reaction of hydroxyl groups on the membrane surface with 2-chloro-2-oxo-1,3,2-dioxaphospholane （COP） followed by the ring-opening reaction of COP with trimethylamine. Chemical differences between the original and the modified membranes were characterized by FT-IR and XPS, It was found that the amount of macrophage adhered on the modified membrane surface is substantially lower than that on polyacrylonitrile （PAN） and PANCHEMA membranes under the same condition, The morphological change of the adherent cell is also suppressed by the generation ofphospholipid moieties on the membrane surface.
文摘To improve the hydrophilicity of polyacrylonitrile-based membranes, sugar moieties were incorporated into acrylonitrile-based copolymers via the radical copolymerization of α-allyl glucoside(AG) with acrylonitrile(AN) with 2,2′-azobis-iso-butyronitrile(AIBN) as the initiator in dimethyl sulphoxide(DMSO). It was found that the yield increased with the increase of the initiator concentration and reaction time, while it decreased with the increase of the monomer molar ratio of AG to AN. Raising the AG proportion in the monomer mixture resulted in the increase of the AG content in the copolymer. M_v of the copolymers decreased with increasing the AG monomer fraction in feed. The copolymers were fabricated into dense membranes and their surface properties were studied by means of the water contact angle measurement and platelet adhesion tests. It was found that the static water contact angle on the membrane decreased significantly from 70° to 33° with the increase of the AG content. The adhesive number of platelets on the membrane surface also decreased significantly with increasing AG content in the copolymers. These results demonstrate that the hydrophilicity and biocompatibility of the acrylonitrile-based copolymer membranes could be improved efficiently by the copolymerization of acrylonitrile with vinyl carbohydrates.
