Nanostructured optical fibre arrays for high-density biochemical sensing and remote imaging

Optical fibre bundles usually comprise a few thousand to tens of thousands of individually clad glass optical fibres. The ordered arrangement of the fibres enables coherent transmission of an image through the bundle and therefore enables analysis and viewing in remote locations. In fused bundles, this architecture has also been used to fabricate arrays of various micro to nano-scale surface structures (micro/nanowells, nanotips, triangles, etc.) over relatively large areas. These surface structures have been used to obtain new optical and analytical capabilities. Indeed, the imaging bundle can be thought of as a “starting material” that can be sculpted by a combination of fibre drawing and selective wet-chemical etching processes. A large variety of bioanalytical applications have thus been developed, ranging from nano-optics to DNA nanoarrays. For instance, nanostructured optical surfaces with intrinsic light-guiding properties have been exploited as surface-enhanced Raman scattering (SERS) platforms and as near-field probe arrays. They have also been productively associated with electrochemistry to fabricate arrays of transparent nanoelectrodes with electrochemiluminescent imaging properties. The confined geometry of the wells has been loaded with biosensing materials and used as femtolitre-sized vessels to detect single molecules. This review describes the fabrication of high-density nanostructured optical fibre arrays and summarizes the large range of optical and bioanalytical applications that have been developed, reflecting the versatility of this ordered light-guiding platform.     

改性UHMWPE纤维/乙烯基酯树脂复合材料的研究

超高分子量聚乙烯纤维在过氧化物引发下,通过硅烷进行接枝改性。研究了改性纤维／乙烯基酯树脂复合材料的界面性能。采用层间剪切强度、扫描电镜、红外光谱(ATRIR)及浸润性测试等分析手段表征了接枝改性的效果。结果表明,经过硅烷接枝改性,改善了超高分子量聚乙烯纤维对乙烯基酯树脂的浸润性,提高了纤维与基体之间的粘结性,使复合材料的层间剪切强度大幅度提高。     

Fluorescence-based fibre optic arrays: a universal platform for sensing

Optical fibres provide a universal sensing platform as they are easily integrated with a multitude of different sensing schemes. Such schemes enable the preparation of a multitude of sensors from relatively straightforward pH sensors, to more complex ones, including artificial olfaction sensors, high-density oligonucleotide arrays, and high-throughput cell-based arrays. Imaging fibre bundles comprised of thousands of fused optical fibres are the basis for an optically connected, individually addressable parallel sensing platform. Fibre optic imaging bundles possess miniature feature sizes (3-10 micron diameter fibres), allowing high-density sensor packing (approximately 2 x 10(7) sensors per cm2). Imaging fibre bundles transmit coherent images enabling combined imaging and sensing, relating the responses monitored by the sensor to observable physical changes. The individual fibre cores can also be selectively etched to form a high-density microwell array capable of housing complementary sized microsensors. The miniature feature sizes facilitate a faster response and more sensitive measurement capabilities. The platform is extremely versatile in its sensing design, allowing the sensing scheme to be tailored to fit the experimental design, whether for monitoring single analytes or more complex multiplexed assays. A number of sensing schemes and applications are described in this review.     

Surface acoustic waves for the characterization of BN-coated fibres observed by Brillouin light scattering

The observation of acoustic phonons located at the surface of uncoated fibres or guided in thin films deposited on fibres by Brillouin light scattering spectroscopy (BLS) is reported. The BLS technique is non-destructive and non-intrusive and is well applicable to non-planar sample geometries. Investigations were carried out on bundles of commercially available carbon fibres, in which a single fibre was 5 m in diameter. With regard to the detected surface acoustic excitations, each fibre can be considered as an infinite halfspace owing to the large ratio of fibre diameter to wavelength. The shear modulus, which is highly relevant for the intended technical application, was determined by measurement of the Rayleigh mode phase velocity of the uncoated fibres. These fibre bundles were coated with boron nitride (BN) in a continuously driven thermal chemical vapour deposition (CVD) process using trimethyl borate and ammonia as precursors. In comparison to carbon, BN is expected to improve the mechanical properties of fibre-reinforced composites such as fracture toughness at high temperatures. The measured velocity dispersion of the Rayleigh mode of this film-on-substrate system permitted the comparison of the shear stiffness of the carbon fibre and of the BN film material. The results evidence the desired effect of a distinct stiffness reduction of the coated fibre relative to the uncoated fibre in the near-surface region. Additional information can be obtained on the homogeneity of the deposition across the whole fibre bundle.     

The surface charge of regenerated cellulose fibres

In this paper the influence of charged species on the sheet strength of viscose fibres was investigated. Four samples of chemical modified viscose fibres, as well as a reference fibre were studied. The swelling of these viscose fibres and the breaking length of hand sheets have been determined. Comparing the results, the influence of both, swelling and surface charge on the bonding force, is evident. The allocation of the charges, induced by cationic starch and Carboxmethylcellulose, has been analyzed by Titration, attenuated total reflection spectroscopy (ATR) and X-ray photoelectron spectroscopy (XPS). Titration was used to make a first estimation of the charge distribution within the fibre. Using ATR and XPS, more detailed information about the surface charge has been achieved. All measurement methods showed a significant amount of charge on the fibre surface.     

Why do we observe significant differences between measured and ‘back-calculated’ properties of natural fibres?

The drive towards sustainability, even in materials technologies, has fuelled an increasing interest in bio-based composites. Cellulosic fibres, such as flax and jute, are being considered as alternatives to technical synthetic fibres, such as glass, as reinforcements in fibre reinforced polymer composites for a wide range of applications. A critical bottleneck in the advancement of plant fibre composites (PFRPs) is our current inability to predict PFRP properties from data on fibre properties. This is highly desirable in the cost- and time-effective development and design of optimised PFRP materials with reliable behaviour. This study, alongside limited other studies in literature, have found that the experimentally determined (through single fibre tests) fibre properties are significantly different from the predicted (‘back-calculated’ using the popular rule-of-mixtures) fibre properties for plant fibres. In this note, we explore potential sources of the observed discrepancy and identify the more likely origins relating to both measurement and errors in predictions based on the rule-of-mixtures. The explored content in this discussion facilitates the design of a future investigation to (1) identify the sensitivity of the discrepancy between measured and predicted fibre properties to the various potential origins, (2) form a unified hypothesis on the observed phenomenon, and (3) determine whether the rule-of-mixtures model (in specific cases) can be improved and may be able to predict properties precisely.     

Characteristics of radiation induced light in optical fibres for portal imaging application

The purpose of this paper is to characterize the radiation induced light in optical fibres to optimise the design of a new Cherenkov detector for portal imaging application in radiation therapy. Experiments were performed using a single optical fibre to evaluate the angle dependence, spectrum and temporal properties of the radiation induced light in the optical fibre in comparison with that of Cherenkov radiation. A theoretical model was also developed to compare with experiments. It has been found that radiation-induced light output from the optical fibre under megavoltage (MV) x-ray irradiation is significantly (about 45 times) higher than that under 100 kVp x-ray irradiation for the same dose rate at the fibre. The angular-dependence, spectrum and temporal properties of the radiation induced light in the optical fibre under MV x-ray irradiation match that of Cherenkov radiation. Different angular dependence and spectrum results from that of previous studies on radiation induced light in optical fibres have also been found. The result of the theoretical model agrees with the angle-dependence measurements.     

Carbon nanotube growth on high modulus carbon fibres: Morphological and interfacial characterization

Carbon nanotubes (CNTs) were grown directly on the surface of carbon fibres, using the catalytic chemical vapour deposition. FeCo bimetallic catalysts were deposited on carbon fibres using a simple wet impregnation method. CNTs were synthesized over the prepared catalysts by the catalytic decomposition of acetylene at 750^oC. The uniform CNT formation on the fibre surface was verified using scanning electron microscopy. Raman spectroscopy was employed to evaluate non‐destructively the CNT growth and the CNT quality. Thermo gravimetric analysis and differential thermal analysis were employed as destructive methods to confirm the spectroscopic data. Single CNT‐coated fibre fragmentation tests were performed to examine the interfacial shear strength (ISS) of the modified fibres. Acoustic emission was employed to monitor the fragmentation process in real time. Thus, the coated fibre structural integrity was assessed together with its stress transfer properties. Polarized optical microscopy was employed to cross validate the acoustic emission data. It was found that the ISS of the nanotube‐reinforced interphase was improved without affecting the fibre mechanical properties. Copyright © 2013 John Wiley & Sons, Ltd.     

Characterization of sugar palm (Arenga pinnata) fibres

The aim of this study was to characterize tensile and thermal properties of sugar palm (Arenga pinnata) fibres obtained from different heights (1, 3, 5, 7, 9, 11, 13, and 15?m) of sugar palm tree. This study has confirmed that in a mature sugar palm tree, degradation was occurred and altered the properties of its fibre. Fibres obtained at the area of live (green) palm frond were found to have a better tensile properties as a result of its optimum chemical composition especially cellulose, hemicelluloses and lignin. For the fibre obtained from the upper part of sugar palm tree, it shows slightly decreasing trend in tensile properties compared to mature fibres. It is due to the fibres are juvenile where their cell walls are progressively built up thus give slightly lower properties than matured fibres. For the fibre obtained from the area of dead palm frond, the fibres are considered to be degraded biologically. It is believed that polymeric chains in microfibrils were broken and their cellulose content was decreased which demonstrated inferior properties (tensile strength, modulus, elongation at break and toughness). The use of such fibre for application as reinforcing fibre in composite is not recommended since the strength of the fibre and composite will be reduced. There were four phases of decomposition of the fibres where the sequence of decomposition started with decomposition of moisture, followed by hemicelluloses, then cellulose and next is lignin while the ash was the last component left. The thermal degradation of these components were found in ranges of 45?C123, 210?C300, 300?C400, 160?C900 and 1723?°C, respectively. Thermogravimetric analysis and derivative thermogravimetric analysis curves showed that the fibre of 1?m showed higher thermal stability than the fibres of 3?C15?m. The different thermal stability for each fibre was due to different chemical compositions especially when the fibre containing high ash content which result in higher thermal stability.     

Interferometric studies on polymer structure

A multiple-beam interferometric method is used to study the change of optical orientation function and molecular structure of nylon-6 fibres due to γ-irradiation under vacuum. It was found that γ-radiation causes alignment to the fibre chains in the direction of the fibre axis, this alignment gives an increase in the optical orientation function. A two-beam interferometric method is used to study the changes in optical orientation function on drawn polypropylene fibres. Empirical formulae are suggested to correlate these changes in the optical orientation function with the dose and with the draw ratio. This study aims to show that the multiple-beam and two-beam interferometric methods can be used to study the changes that take place in polymers and fibres by irradiation or drawing.     

Effects of electrochemical and plasma treatments on carbon fibre surfaces

This paper summarizes the chemical changes induced on carbon fibre surfaces (examined by X-ray photoelectron spectroscopy, XPS) by a variety of electrochemical treatment in aqueous electrolytes together with the improvements in fibre/resin bonding in the corresponding composite materials. It was found that there was no correlation between the amount of chemical functionality introduced onto the fibre surface and the fibre/resin bond strength, i.e. chemical bonding does not play a major role in fibre resin adhesion. This does not rule out the possibility of chemical bonding between the fibre and resin—it simply implies that it is not the governing factor. It is suggested that the immediate surface concentration of chemical groups is too low to make a significant contribution. To tailor interfacial properties it would be desirable to promote chemical bonding between fibre and matrix. The use of a specially designed plasma treatment cell has led to an increase in the surface concentration of chemical groups ( C OH, hydroxyl) that have the potential to react chemically with the resin. By exploiting grazing angle data taken from XPS analysis, it is shown that changes in the chemical nature of the fibres only occurs in the outermost layers, whereas the electrochemical reaction proceeds well into the fibre sublayers. Selective introduction of nitrogen-containing functionality (such as amines,  NH₂) has been achieved. The reactivity towards a particular plasma is shown to be largely dependent on the structure of the fibre surface. The number of C/N groups produced on higher modulus fibres was undesirably low. Their concentration was increased by biasing the fibres to a negative potential (10–30 V) during plasma exposure.     

Thermal analysis of fibre forming polymers

Different levels of fibre technologies and application, from synthesis to degradation has been studied using the methods of thermal analysis. Recent results of these studies on synthetic and natural fibres are summarized. The effect of chemical and physical modification of polyolefin fibres as well as the synthesis of polymer emulsion used as additive in fibre technologies could be followed by DSC, DMA, TG methods.     

Comparison of molecular orientation and mechanical properties of lyocell fibre tow and staple fibres

Samples of lyocell fibres were taken in the form of filaments from fibre tow of potentially infinite length and in their final condition of staple fibres. Mechanical testing showed comparable tensile strength, but a 50% lower modulus of elasticity for staple fibres and a higher elongation at break compared to filaments from fibre tow. Structural investigation by means of synchrotron wide angle X-ray scattering and birefringence measurement revealed a significantly lower degree of preferred orientation together with less fibre straightness for staple fibres than for filaments. It is concluded that plastic deformation during the processing of staple fibres from filaments induces permanent changes in the orientation of cellulose chains in the fibres, which in turn is responsible for the observed differences in mechanical performance.     

Study of cellulosic fibres morphological features and their modifications using hemicelluloses

The microfibrilar structure and the morphology of the fibre are some of the most important characteristics that determine fibre performance during yarn making. This article is focused on understanding of morphological features of manmade cellulosic fibre and exploring an alternate way to alter fibre morphology. It is observed that though the chemical nature of different types of cellulose fibres viz. viscose, modal and lyocell is same; different processing routes lead to different cross-section and morphologies of fibres which leads to their characteristic properties and spinning behavior. A novel way is attempted to alter the fibre morphology of viscose fibre by changing the fibre regeneration kinetics and molecular weight distribution through addition of low molecular weight and branched structured hemicelluloses in spinning dope. Addition of hemicelluloses in the spinning dope prior to spinning and regeneration of viscose fibres is found to alter the morphology of the fibres without affecting tensile properties of the fibres.     

The porous structure of pulp fibres with different yields and its influence on paper strength

The porous structure of the interior of papermaking fibres is a well-known important property of the fibres. Changes of this structure will influence tensile and burst strength of paper formed from the fibres and a change in pore size of the pores within the fibre wall is also important for the ability of molecules to diffuse in and out of the fibre wall. Relevant examples of this latter effect are the removal of lignin during cooking and the addition of performance chemicals during papermaking. In this paper, pore sizes and the pore size distribution of unbleached softwood fibres have been studied. A well-characterised fibre material consisting of laboratory cooked spruce and pine pulp of various lignin contents was used. Pore size and pore size distribution were measured by studies of the relaxation behaviour of ²H in fibres saturated with ²H₂O. Beside this the total and surface charge of the fibres were also measured together with strength properties of papers from unbeaten fibres. For both pulps, there is a maximum in pore radius at a yield around 46%. Calculations of fibre wall volume from water retention values and yield levels show that there is a discontinuity in pore radius as a function of the fibre wall volume around a yield of 51%. It is suggested that this discontinuity is caused by the breakdown of the hemicellulose/lignin matrix within the fibre wall at this yield level. The strength of the papers formed from the fibres shows a correlation with the surface charge of the fibres. Based on the change in surface charge with yield and the change in total charge with yield, this correlation is suggested to be due to an opening up of the external part of the fibre wall. This stresses the importance of the chemical composition and physical structure of the outer layer of the fibre wall.     

Rapid Detection of Foot-and-Mouth Disease Virus with Optical Microchip Sensors

Rapid identification of infectious disease pathogens such as foot-and-mouth disease virus (FMDV) during new outbreaks of disease is of fundamental importance in disease control. SpectroSens^TM optical microchip sensors demonstrating rapid, label-free detection of FMDV are presented; these contain multiple high-precision planar Bragg gratings and function as low-cost, robust refractive-index sensors. Sensor selectivity to FMDV is imparted by functionalising the top-surface of specific sensing channels with anti-FMDV monoclonal antibodies (mAbs). Selective binding of cognate antigens within the test sample to surface-immobilised FMDV mAbs results in localised changes in refractive index within specific sensing channels; these antibody-antigen interactions manifest as increases in wavelength of light reflected from the multi-channel sensor chip (light is coupled into and out of the chip via optical fibres). Selective identification of FMDV within minutes of sample introduction has been demonstrated by referenced measurement of changes in sensor reflected wavelength from anti-FMDV channels against sensor controls; simplified ‘snap-shot’ assay data are displayed in the form of a simple yes/no readout using a robust, hand-portable device, with further semi-quantitative information available to the ‘super-user’. The characteristics of the SpectroSens^TM multiplexed detection platform highlight its potential for in-field detection of foot-and-mouth disease and prospective expansion into diagnoses of other infectious veterinary diseases.     

Investigation of nylon-6 fibre structure interferometrically

Multiple-beam Fizeau fringes are used to study the changes in optical properties of Nylon-6 γ-irradiated fibres. Changes in fibre structures due to drawing have been studied using two-beam interference. Some structural parameters such as optical orientation function and electric polarizability difference (Δ/3₀) were determined. Δ/3₀ is found to be constant and depends only on the fibre structure. The generalized Lorantz-Loranz equation given by de Vries is used to determine Nylon-6 fibre structural parameters. Comparison between the results and when using Lorantz-Loranz equation are given. Refractive index profiles also can help in fibre investigations.     

Imaging of the formerly bonded area of individual fibre to fibre joints with SEM and AFM

Besides the determination of the force and the energy needed to break individual fibre to fibre joints, the investigation of the formerly bonded area (FBA) is of essential importance to learn more about the failure mechanisms of fibre–fibre bonds in general. In this study the surfaces of paper fibres and the FBA of fibre–fibre joints after the determination of the breaking force as well as the bonding energy were analysed by means of low voltage scanning electron microscopy and atomic force microscopy. A comparison between the contact zone of fibres broken at different loading rates as well as under cyclic loading showed that there seems to be no significant difference in the appearance of the FBA in these cases. Only minor delamination of the cell wall could be found in the bonding zone, which indicates no mechanical interlocking of fibrils in the bonding zone. Furthermore, it is shown that some glues used for specimen preparation of fibre–fibre bond strength measurement are forming a glue film on the fiber surface and migrate into the bonding region.     

Endoxylanase action towards the improvement of recycled fibre properties

The nature of recycled paper fibres varies widely. Those fibres contain high amounts of heteroxylans and lignin besides cellulose. In order to study the potential effect of xylanases on the quality of recycled fibres, chemithermomechanical pulp fibres (CTMP) are used as model substrates owing to their high content in non-cellulosic components. It has been found that the morphology of CTMP fibres changes by means of xylanase treatment. Treatments of CTMP fibres with an endoxylanase result in an improved surface area of the fibres by fibrillation, without shortening the fibres. The chemical composition of the surfaces of the fibres changes and an augment in surface hydrophilicity as a result of the removal of lignin and extractives associated to the xylan backbones is observed. Experimental results are in agreement with the findings when studying the chemical composition of the fibres’ surfaces: the xylan backbone is removed by the action of the endoxylanase, resulting in fibre fibrillation; further hydrolysis of released xylan chains proceeds in the bulk down to the monomer xylose.     

Investigating the provenance of un-dyed spun cotton fibre using multi-isotope profiles and chemometric analysis

The analysis of un-dyed spun cotton fibres can be challenging within a forensic science context where discrimination of one fibre from another is of importance. Conventional microscopic and chemical analysis of these fibres is generally unsuccessful because of their similar morphology. In this work we have explored the potential of isotope ratio mass spectrometry (IRMS) as a tool for spun cotton fibre analysis in an attempt to reveal any discriminatory information available. Seven different batches of un-dyed spun cotton fibre from four different countries were analysed. A combination of the hydrogen and oxygen isotopic data facilitated the correct association of the samples, demonstrating, for the first time, the applicability of IRMS to fibre analysis in this way.