A comparison of polyelectrolyte complexes and multilayers: Their adsorption behaviour and use for enhancing tensile strength of paper
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作者:
Ankerfors, Caroline
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KTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
Eka Chem AB, SE-44580 Bohus, SwedenKTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
Ankerfors, Caroline
[1
,2
]
Lingstrom, Rikard
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KTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, SwedenKTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
Lingstrom, Rikard
[1
]
Wagberg, Lars
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KTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, SwedenKTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
Wagberg, Lars
[1
]
Odberg, Lars
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KTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, SwedenKTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
Odberg, Lars
[1
]
机构:
[1] KTH, Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
This paper compares the adsorption behaviour and paper-strength-enhancing properties of polyelectrolyte complexes (PECs) and polyelectrolyte multilayers (PEMs) of polyallylamine hydrochloride and polyacrylic acid. Model adsorption experiments using SPAR (stagnation point adsorption reflectometry) and QCM-D (quartz crystal microbalance with dissipation) showed that the amount of complexes adsorbed was lower than the amount adsorbed when forming a multilayer using the same polymer system. From these experiments, in combination with AFM and ESEM imaging, it was concluded that the PEC adsorption stopped before full surface coverage was reached. Tensile testing of handsheets treated with PECs and PEM showed a significant increase in both tensile index and strain-at-break using both systems. The largest strength improvement was achieved with the fibres treated with the largest number of PEMs, but the largest effect per adsorbed amount of polymer was achieved by PEC treatment.