Solid wood joints by in situ welding of structural wood constituents

Holzforschung ◽  
2004 ◽  
Vol 58 (1) ◽  
pp. 45-52 ◽  
Author(s):  
B. Gfeller ◽  
A. Pizzi ◽  
M. Zanetti ◽  
M. Properzi ◽  
F. Pichelin ◽  
...  

Abstract Mechanically-induced wood flow welding, without any adhesive, is here shown to rapidly yield wood joints satisfying the relevant requirements for structural application. The mechanism of mechanically-induced vibrational wood flow welding is shown to be due mostly to the melting and flowing of the amorphous polymer materials interconnecting wood cells, mainly lignin, but also some hemicelluloses. This causes the partial detachment of long wood cells and wood fibres and the formation of an entanglement network in a matrix of melted material which then solidifies. Thus, it forms a wood cell/fibre entanglement network composite having a molten lignin polymer matrix. During the welding period, some of the detached wood fibres no longer held by the interconnecting material are pushed out of the joint as excess fibre. Cross-linking chemical reactions of lignin and of carbohydrate-derived furfural also occur. Their presence has been identified by CP-MAS 13C NMR. These reactions are, however, relatively minor contributors during the very short welding period. Their contribution increases after welding has finished, explaining why relatively longer holding times under pressure after the end of welding contribute strongly to obtaining a good bond.

InfoMat ◽  
2021 ◽  
Author(s):  
Ramin Rojaee ◽  
Samuel Plunkett ◽  
Md Golam Rasul ◽  
Meng Cheng ◽  
Vahid Jabbari ◽  
...  

2012 ◽  
Vol 12 (9) ◽  
pp. 1220-1231 ◽  
Author(s):  
Adrian Sulistio ◽  
Anton Blencowe ◽  
Jiapei Wang ◽  
Gary Bryant ◽  
Xiaoqing Zhang ◽  
...  
Keyword(s):  

1997 ◽  
Vol 62 (8) ◽  
pp. 1254-1262 ◽  
Author(s):  
Bernd Wrackmeyer ◽  
Hans-Jörg Schanz

The formation of organo substituted 1-carba-arachno-pentaborane(10) derivatives is shown to proceed in high yield via in situ generated 1,1,1-tris(diethylboryl)propane (2) from diethyl(propyn-1-yl)borane (1) by hydroboration with an excess of diethylborane (hydride bath). In the hydride bath, exchange reactions between 2 and other geminal bis(diethylboryl)alkanes take place until the carbaborane skeleton is formed. If tris(diethylboryl)methane is used under the same conditions, the corresponding 1-carba-arachno-pentaborane(10) derivatives 11 and 12 are formed in mixture with other unknown boranes or carboranes. 11B and 13C NMR data are presented to allow for straightforward identification of the 1-carba-arachno-pentaboranes(10).


2018 ◽  
Vol 42 (13) ◽  
pp. 11023-11030 ◽  
Author(s):  
Lulu Liang ◽  
Li Nie ◽  
Minjuan Jiang ◽  
Fusheng Bie ◽  
Linjun Shao ◽  
...  

Chitosan composite superfine fibers with a diameter of 321 ± 99 nm were prepared by electrospinning with PEO as the co-spinning polymer and itaconic acid as the in situ cross-linking agent.


2018 ◽  
Vol 57 (50) ◽  
pp. 17048-17057 ◽  
Author(s):  
Yanping Huang ◽  
Nianhua Dan ◽  
Weihua Dan ◽  
Weifeng Zhao ◽  
Zhongxiang Bai ◽  
...  

2011 ◽  
Vol 23 (6) ◽  
pp. 1212-1216 ◽  
Author(s):  
Meike M. Mostegl ◽  
Barbara Richter ◽  
Nora Dinhopl ◽  
Herbert Weissenböck

Chromogenic in situ hybridization (ISH) is a commonly used tool in diagnostic pathology to detect pathogens in formalin-fixed, paraffin-embedded (FFPE) tissue sections. Prolonged formalin fixation time was identified to be a limiting factor for the successful detection of nucleic acid from different pathogens, most probably due to the cross-linking activity of formalin between RNA, DNA, and proteins. Therefore, in the current study, the influence of formalin fixation time on ISH signal intensity of 2 viral ( Porcine circovirus-2 [PCV-2] and Porcine respiratory and reproductive virus [PRRSV]) and 2 protozoal agents ( Cryptosporidium serpentis and Tritrichomonas sp.) was evaluated. Tissue samples were fixed in 7% neutral buffered formaldehyde solution, and at defined intervals, pieces were embedded in paraffin wax and subjected to pathogen-specific ISH. For all 4 pathogens, the signal intensity remained comparable with the starting ISH signal for different periods of fixation (PCV-2: 6 weeks, PRRSV: 23 weeks, C. serpentis: 55 weeks, Tritrichomonas sp.: 53 weeks). Thereafter, the signal started to decline until loss of nucleic acid detection. The influence of increased proteinase K concentrations for inverting the formalin-induced cross-linking activity was examined compared with the standard protocol. With all 4 infectious agents, a 4-fold proteinase K concentration restored the ISH signals to a level comparable with 1 day of fixation. In conclusion, the influence of prolonged formalin fixation on the intensity of detected ISH signal highly depends on the analyzed infectious agent and the pretreatment protocol.


1992 ◽  
Vol 271 ◽  
Author(s):  
Kevin J. Thorne ◽  
Stephen E. Johnson ◽  
Haixing Zheng ◽  
John D. Mackenzie ◽  
M. F Hawthorne

ABSTRACTTo prepare new polycarbosilane polymer precursors with high solubility and the capability of UV cross-linking, commercial polycarbosilane was modified by a chemical route. These modifications involved AlCl3 catalyzed chlorination reactions of polycarbosilane's Si-H bonds. The resultant Si-Cl bonds were substituted by a reaction with sodium acetylyde to form Si-C=CH ligands. These ligands are suitable for controlled, free radical initiated cross-linking of the polycarbosilane polymers. The increase in molecular weight should allow for increased Tg's and the retention of polymer pre-forms. In this report, the chlorination of the polycarbosilane polymer and the substitution reactions of polycarbosilane were examined with IR, 29Si and 13C NMR spectroscopy. In addition, the retention of polymer pre-forms were analyzed after UV exposure and inert atmosphere pyrolysis.


2018 ◽  
Vol 8 (5) ◽  
pp. 178-183
Author(s):  
Manish Kumar ◽  
Hemant K. Sharma

The objective of this study is to prepare nanogels were prepared via charged gellan gum. It was prepared by in situ cross linking reaction between two oppositely charged materials by green method without use of chemical cross linking agents. The prepared nanogels were characterized by Dynamic light scattering, scanning electron microscopy, differential scanning calorimetry and X- Ray diffractometry. The prepared formulation had average particle size of 226 nm with polydispersity index of 0.3. The doxorubicin loaded nanogel demonstrated sustained release for 20 h. The prepared nanogels were hemocompatible and cyctocompatible as revealed by hemocompatibility and MTT assay respectively. All results confirmed that these nanogels can be used for cancer treatment. Keywords: Nanogel, Chitosan, Gellan gum, Doxorubicin, Cancer.


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