AGS Benchmarking
Initiative gets underway
After several false starts, the Business Practice WG has
finalised plans for an AGS initiative to evaluate the quality of site
investigations undertaken by Members. This will be the first time that an
attempt has been made to qualify site investigation practice and the results are
eagerly awaited.
The WG has identified 11 Key Performance Indicators (KPIs)
and subsidiary headings:-
-
Appointment (Personnel, Responsibilities)
-
Preparation (Desk Study, Walkover Survey, Reports)
-
Design (SI Design, Laboratory Testing)
-
Risk Management (Risk, Availability of Information)
-
Procurement (GI Procurement Route, SI Award, Method of
Measurement, Conditions of Contract, Specification)
-
Management (Project Management, Quality Management,
Environmental Management)
-
Supervision
-
Reporting (Factual)
-
Reporting (Interpretative Report, Ground Model)
-
Outcome
-
Client Satisfaction
All AGS Members have been invited to participate. The number
of projects that each participant will be asked to score will depend on the
number of companies that agree to take part but will not be more than 10 (and
probably less). It will not be necessary to identify the project being scored
and the score of individual projects will not be revealed.
It is intended that once the initial benchmark has been set
the exercise will be repeated annually to monitor changes in standards.
It is not too late to register as a participant. Please
contact Jo Pascoe (jo@ags.org.uk) for further details.
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MCERTS
The Environment Agency's Monitoring Certification
Scheme for the Chemical Testing of Soils:
What it is. How it affects you. What you need to do.
MCERTS Monitoring Certification Schemes were first introduced
in industrial sectors with regulated processes that resulted in stack emissions.
The scheme requires those companies to deliver monitoring results that are
"valid, reliable and accurate". To get to this position depends on
using the appropriate resources - correct test methods, competent personal,
accredited organisations and suitable equipment and planning.
The MCERTS scheme for chemical testing of soils was
introduced by the Environment Agency to support their regulatory activities and
make informed, quality assessments on the management of contaminated land under
a number of regimes, including, Part IIa of the Environmental Protection Act
1990, Pollution Prevention and Control Regulations 2000 and the Waste Management
Licensing Regulations 1994.
The scheme is applicable to all testing laboratories and
procurers of analytical services, where results generated for the chemical
testing of soil are submitted to the Agency. In order to gain accreditation on
the scheme, laboratories are required to have their processes, essentially test
methods, in a quality management framework, by both the United Kingdom
Accreditation Service (UKAS) to the international standard ISO 17025 and also
MCERTS requirements.
There are increasing pressures on businesses to comply with
Environment Agency regulations and European and international standards. Using a
laboratory with MCERTS accreditation alleviates some of this pressure because it
guarantees the proper use of suitable methods, standards, services and
equipment, trained and qualified personnel, quality assurance and quality
control all leading to reliable data. MCERTS accreditation also assures users
that the laboratory meets performance standards set out in current international
standards and the growing requirements of EC directives.
Failure to meet the regulations can be costly, both
financially and to a company's reputation. An MCERTS accredited laboratory
assures the user that they have met standards in a number of areas including:
-
The selection and validation of test methods
-
Sampling pre-treatment and preparation
-
The estimation of measurement uncertainty
-
Participation in proficiency testing schemes
-
The reporting of results and information
The benefits of the scheme include:
-
Providing assurance to stakeholders of the quality of
data from testing
-
A level playing field, based on the Agency's
requirements, is established
-
Identifying that the chemical testing of soil is a
critical component in producing defensible data for regulatory purposes.
In order to guarantee reliable data from the chemical testing
of soils and therefore reassurance that risks are minimised, procurers of
testing should:
-
Ensure the chemical analysis results submitted to the
Agency for regulatory purposes conform to MCERTS requirements.
-
Check that the laboratory conducting the testing has
MCERTS accreditation for all the parameters requiring analysis.
Accreditation is given on a parameter-by-parameter basis. If they do not
have the correct accreditation sub-contracting of the test required to
another MCERTS laboratory may be required. If a suitable laboratory does not
appear to be available, contact the Environment Agency for advice.
-
Check that the test methods employed by the laboratory
are appropriate and fit for purpose in terms of the parameter, the Critical
level of interest (CLI) and the matrix. The CLI may be a soil guideline
value or a regulatory limit.
-
Check with the laboratory that the sampling processes,
preservation and transportation are appropriate.
-
In collaboration with your chosen laboratory, have
complete audit trails available that address aspects such as sample
location, depth of sample, date and time of sample, reference identity and
the laboratory used.
The MCERTS scheme for the chemical testing of soils was
phased in, but has been fully operational since 1 March 2005. Therefore, all
data for regulatory purposes should now be to the MCERTS standard. Laboratories
and the procurers of testing need to work together to ensure that the test data
provided meets the requirements and satisfies the needs of the ultimate client.
Cliff Billings Group Technical & Quality Manager STL UK
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EA's position on MCERTs
From 1st March 2005, the Environment Agency has required
accreditation to our Monitoring Certification Scheme (MCERTS) where laboratory
soil testing results are submitted to us as part of a regulatory regime for
which we have statutory responsibility.
We strongly recommend that MCERTS accredited methods are used
for soil testing in activities to do with site remediation, whether carried out
on a voluntary basis or to comply with planning requirements. This is
particularly important in relation to any waste management issues on the site.
Jackie Harrison Environment Agency
Contaminated Land Working Group Meetings
In recent meetings of the Contaminated Land Working Group, it
has been clarified that the EA is a consultee but not a Statutory Regulator for
planning applications. This means that MCERTs data may not always be required at
the planning stage. Although the EA recommend MCERTS, the final decision is up
to the Local Authority.
Some AGS Members feel that all tests should be to MCERTS so
that the reports can be used at a later date. At present, the EA is expected to
take a pragmatic approach to historical data obtained before the introduction of
MCERTS and take account of whether the laboratory is now accredited, and other
relevant factors. However, this may not always be the case, particularly for
data collected after March 2005, and the need to 'future proof' data should be
seriously considered.
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Meet NHBC Requirements
with MCERTS
The NHBC welcomes MCERTs accredited testing and supports it's
use in association with robust and representative soil sampling strategies when
investigating sites affected by contamination. It brings transparency and
consistency to the analytical testing techniques and encourages discussion
between the consultants and testing laboratories which can only be a positive
step forward.
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Contaminated Land
Analysis - Introducing Doubt Into An Uncertain World
Let's be honest, to most of us in the ground engineering
community, chemistry is something of a black art. It's a subject we never
properly understood at school and certainly not one we intended to revisit in
our professional capacities. We can muddle through the uncertainties of soil
mechanics and a few of us claim a vague understanding of finite element
analysis. Imagine our horror therefore when chemistry abruptly re-entered our
world in the form of contaminated land. Our inattention and tomfoolery at the
back of class has suddenly come back to bite us. Hazy schoolday recollections of
sodium fizzing around in the sink or the exploding magic green fountain aren't
going to get us out of this one.
And it gets worse! Chemistry is no longer even just a
disagreeable side issue for many of us and on many developments it sits,
gloating, athwart our critical path, knowing full well that not only do we not
know the answer, we are often unsure of the right questions to ask as well.
So where is our white knight, to whom can we turn for help
and enlightenment? In the past we might have turned to our laboratory for help.
However over the last 15 years or so there has been a complete rationalisation
of the chemical testing market. Laboratories have tended to become bigger and
more automated, offering cost effective analysis but consequently less
consultancy support. Intense competition amongst the key players means that
margins are so tight there is little room in modern production line chemistry
for added value services. Testing has become a numbers game.
There are now several degrees of separation between the
engineer and the chemist. Yet we are in fact very similar in one key respect and
it is here that we close the circle. They don't understand what we do and we
don't understand what they do.
Laboratories must adopt operating practices which enable them
to make a profit under conditions of intense price competition. Their choices
fundamentally affect the quality and reliability of the data they produce. We
don't even know what questions to ask and many laboratories in turn are less
than forthcoming in disclosing the limitations of their data. We work together
in blissful ignorance even though our interaction (or lack of it) has a critical
influence on the quality of the data they produce and we then use.
Accreditation schemes such as UKAS, compliance schemes (e.g.
Contest, WASP) and the recently developed MCERTS scheme championed by the
Environment Agency are all designed to address quality issues in laboratory
testing. However all have significant limitations which are not readily apparent
and are certainly not advertised to a largely ignorant consumer.
So what's the problem. Well the example in box 1 below
illustrates this nicely. In it we have simulated total soil cadmium data from
two simulated laboratories. One of the simulated laboratories is a reputable,
highly regarded outfit with excellent quality control and in the case of our
simulated sample it has if fact got an answer which approximates to the true
value. The only downside is that quality costs and it charges £1 to undertake
the analysis. The other laboratory has a less robust quality system and the cost
savings allow it to charge just 50p for a cadmium determination. However its
reported total cadmium concentration is in fact in this case woefully
inaccurate. See if you spot the wrong answer.
|
Laboratory |
A |
B |
|
Total Cadmium |
617.2 mg/kg Cd |
617.2 mg/kg Cd |
The problem is of course that you can't tell by looking
whether data is reliable or not. Because buyers of chemistry are largely
ignorant of chemistry, and the product we buy does not readily reveal its
quality, then the key differentiator becomes price. Whilst there is an industry
bottom line which we might say is policed by accreditation schemes such as UKAS,
we should not be naïve enough to believe that this is in anyway a guarantee of
a right answer. Now the punch line, and you fanatically precise engineers are
not going to like this. We should recognise that even good data is not 'correct'
in the right and wrong sense and that some degree of uncertainty is inherent in
every result. Sometimes this uncertainty is very large indeed, 617.2 mg/kg could
actually mean anything from about 80-1000 mg/kg and that should give us all some
food for thought.
So what are the questions we should ask. Well here are some
important ones for starters.
Basis, basis, basis
The basis on which you send your sample to the laboratory
could be as follows. It is a cold and wet day. The wind is making life difficult
and you are worried about getting caught in the traffic if you don't get off
site soon. You shovel a couple of kilograms of rubble into the bag and leave the
bag by the gate for the laboratory to pick it up sometime later in the week. In
a couple of weeks the laboratory (UKAS accredited as the contract specified)
reports back to you and you are relieved to see the thiocyanate content is 24.7
mg/kg, just below your limit of 25 mg/kg. You're in the clear, you can sign the
site off - or can you? Have you considered these questions?
How was the sample prepared, and by whom?
What is the precision and bias of the method used?
On what basis are method precision and bias measured?
On what basis is the data reported?
On what basis is your acceptance criterion calculated?
Sample Preparation
We can't emphasise enough how important initial sample
preparation is. If it is not right then everything that comes after is wrong.
Unfortunately good sample preparation is expensive, labour intensive and very
repetitive - it is simply not fashionable and therefore often neglected. You
will almost always find the least qualified staff in a laboratory carrying out
the most important function - sample preparation.
Accreditation schemes accredit results and sample preparation
does not produce a result. It is debatable therefore whether sample preparation
falls within the scope of accreditation. Imagine that - you use a UKAS
accredited laboratory and their single most important operation is not actually
capable of being accredited and is carried out by the least qualified personnel
in the company.
The Quality Control Con
Laboratory quality control focuses on the instrumental side
of the analysis. QC data is usually generated from a point after samples have
been prepared for analysis. Prepared QC samples or certified reference materials
are finely ground, dry, inherently homogenous materials. Real samples are sun
drenched, windswept, dirty, heterogeneous lumps. Don't believe, therefore, that
quoted QC data will necessarily bear any resemblance to that achievable in your
samples.
For example the QC data for samples which are normally
analysed wet (like cyanide) may in fact be determined on dry, ground reference
soils which are spiked immediately before analysis. Doing it this way ensures
excellent QC data but doesn't really relate all that well to the true bias and
recovery one might get from a mixed, wet contaminated soil.
Precision, bias, repeatability &
uncertainty
Each measurement a laboratory makes is subject to any number
of errors. Good laboratories minimises the impact of such errors by sound
methodology and quality control procedures. You cannot however eliminate
uncertainty altogether and a knowledge of uncertainty could be critical to your
remediation scheme.
For example if you have a clean up criteria of 2500 mg/kg of
mineral oil on a scheme and your sample shows a concentration of 2000 mg/kg you
might be forgiven for breathing a sigh of relief. If you knew that the true
precision of the analytical method is more like +/- 100% you might have cause to
re-appraise your hasty signing off of the site.
Bias, or recovery is, in simple terms a measure of the amount
you get out knowing what you originally put in. For example a laboratory quotes
a UKAS accredited method recovery for DRO as 95%. Fine you think a 95% recovery
is very good, and the method is UKAS accredited. What you don't appreciate is
that the recovery is quoted on a reference sample that has been dried and finely
ground. In other words the recovery quoted does not account for any volatiles
lost during drying and grinding.
We can however welcome the (relatively) new MCERTS scheme
championed by the Environment Agency in so far as precision and bias data should
now accompany all results of analysis.
How is data actually reported
Understanding the basis for reporting is really, really
critical. Some samples are analysed wet, some dry, some with stones removed,
some without. Some data is reported dry and some wet, some whole and some just
on the fines. Data on the same sample may be reported on a different basis. Do
you know on what basis your samples are analysed and reported? Do you know on
what basis the acceptance criteria you use (CLEA, Dutch) are generated?
The example below illustrates this point demonstrating the
range of total mercury values you can get depending upon how you choose to
express the data or how that laboratory chooses to prepare your sample.
|
A 100g sample of a contaminated clay is submitted for
total mercury analysis. It contains 500ug of mercury, and is composed of
the fractions set out below. For this example we assume (fairly
reasonably) that all of the mercury is present in the fines. Our
acceptance criteria are the CLEA Soil Guideline Values of 8 mg/kg Hg for
residential uses with plants and 15 mg/kg Hg for residential uses without
plants. |
|
Soil fines (less than 2mm diameter) |
30 grams |
|
Stones (2-10mm diameter) |
20 grams |
|
Stones (greater than 10mm diameter) |
25 grams |
|
Water |
25 grams |
|
Data reported on:- |
Result (mg/kg Hg) |
CLEA 8
SGV |
CLEA 15
SGV |
|
Whole sample |
5.0 |
pass |
pass |
|
Fines, dry |
16.7 |
fail |
fail |
|
Whole, dry |
6.7 |
pass |
pass |
|
<10mm, dry |
10.0 |
fail |
pass |
|
<10mm, wet |
6.7 |
pass |
pass |
The example illustrates a huge variation in 'right' answers
which completely span the selected acceptance criteria. It also reveals that the
same (or very similar answers) can be obtained by using completely different
assumptions - a whole dry basis being very similar to a <10mm wet basis in
this example. What is more worrying is that the fines dry result (arguably the
most common way of determining mercury in soil) is over three times higher than
the result expressed on the whole sample (arguably the true result).
Sample Homogeneity
We all know that reliable data depends upon the sample from
which it was extracted. We all also know how difficult it can be to take
representative samples from very mixed fill and contaminated ground. The
apparent precision of laboratory data can be very misleading. In reality a
result of 645.37 mg/kg lead (as Pb) doesn't actually mean that the horizon we
sampled contains a concentration of 645.37 mg/kg lead. The problem is we don't
know what it means because we haven't estimated the variability of the sampled
horizon and we haven't got a clue about the limitations of the techniques the
lab uses to prepare, extract, analyse and then correct the raw data to produce
the reported result. Engineers who are used to dealing with relative certainties
would be horrified to learn that the true precision of chemical data is very,
very poor. In many cases the best you could expect might be orders of magnitude.
Conclusions - The Key Questions
There is no doubt that the reliability of the analytical data
our industry routinely uses is seriously limited. There is also no doubt that
many (perhaps most) practitioners don't realise this. This is not because the
laboratories are producing poor quality work. Rather it is a combination of the
uncertainty inherent in sampling and analysis coupled with the limitations a
price driven market places upon laboratories. Factor in a lack of understanding
on both sides of the effect (or even existence) of such limitations and it is
easy to see that we can easily find ourselves skating on thin ice without even
realising it.
What are the answers then? Well the answers are really a
series of questions we should routinely ask ourselves when assessing our
methods, our laboratories and their data.
1. Laboratories broadly use the same analytical equipment.
What gives to allow some laboratories to be a lot cheaper than others? 2. What
are the limitations of the selected analytical method? There are always
limitations. Do they matter in this case?
3. Absolutely critical. What is the basis on which my data is reported? Does it
match the basis on which my acceptance criteria are calculated?
4. Is the laboratory QC data realistic or has it been generated in ideal
conditions using ideal samples which are unlikely to represent the conditions on
my site.
If you can make a reasonable attempt at answering these
questions you will be a long way to understanding the basis on which your data
has been generated and in turn you will be reasonably confident when
interpreting your data and able to take due account of the uncertainty that
exists in your data.
If you can't immediately answer these questions then you
don't know the basis on which you are interpreting your data/running your
computer model/applying your acceptance criteria/remediating your site/providing
your client with a collateral warranty. And it's as fundamental as that.
Richard Puttock Partner
Michael Dinsdale Associate
Peter Brett Associates
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Eurocode EC7 National
Application Document NAD
The Ground Forum has received a report that work to prepare a
National Application Document (NAD) for Eurocode 7 (EC7) has been delayed and
impeded because of lack of funding.
This could have serious implications for the Uk if the NAD
for EC7 is not available by January 2007, then EC7 will have to be used in the
UK in its current format. This will mean that all geotechnical design in the UK
will have to be undertaken using all of the published design methods in EC7.
Also, each of these design methods will have to use the general European design
parameters, not parameters that have been calibrated for UK design and
construction practice, and for UK ground conditions.
The benefit of having the NAD for EC7 will be to reduce the
number of design methods applicable for the UK. This will have the obvious
result that design time, and thus cost, will be lower with the implementation of
the NAD, than without it.
In addition, without UK specific design parameters published
in a NAD for EC7, it is likely that designs will either be more safe compared to
those produced by current design practice (resulting in uneconomic designs for
UK clients) or will be less safe compared to those produced by current design
practice (resulting in potential construction failures and associated loss of
confidence by the public and UK clients).
It is the view of The Ground Forum that the publication of a
National Application Document for EC7 is essential before January 2007.
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PID Instruments: Read the Manual
- Understand the Risks
The use of Photo Ionisation Detectors or PID's to delineate
hydrocarbon, or solvent, plumes is common practice these days. Since its
introduction to the UK in the early 90's the technique has won common acceptance
and many equipment hire companies have offerings from various manufacturers.
Many practitioners recognise the need for achieving adequate
calibration of the instrument relative to the material being tracked. The
commonly recognised difference is that of the response factors between petrol
mixtures and diesel fuels. The later material responds far less strongly even to
high energy lamp instruments and the results need to be interpreted accordingly.
Most manufacturers publish correction factors that can be applied to the
instruments response relative to other solvents such as those historically used
as dry cleaning or degreasing fluids.
For general purpose use there may not be a major risk in
terms of business loss prevention; provided plume delineation can be achieved,
professional judgements can be applied in the normal way in terms of the area of
ground affected. However, there is one operational risk that may be problematic,
and poorly understood by a lot of users, this is the impact of humidity.
RAE systems, the makers of a commonly used instrument, assert
that at 60% humidity only 80% of the true atmospheric response may be achieved.
Clearly this is problematic if the instrument is being used to provide safety
critical data during drilling, other ground works, or if the solvent/substance
being studied is a 'low responder'.
There are, of course, other factors which need to be taken
into consideration in this respect, such as: extension tube length; and the
creation of critical alarm set points for mixtures of solvents.
RAE Systems publish a host of free literature which enhances
the safety critical and other uses of data obtained from PID instruments in
general; as well as their own products. This information can be found at:
http://www.raesystems.com/AppTech_Notes/TN .
Loss Prevention Measures
The following are some loss prevention measure which should
be considered:
1. Obtain, and study, the manufacturer's supplementary
product literature.
2. Do not rely entirely on what the hire company has
provided; they will only supply what is needed to ensure the equipment operates
as intended. The instrument output is for user interpretation.
3. Ensure that members of staff using the equipment have
read, and understand, the instrument manual.
4. Ensure that staff members using the equipment are
qualified to deal with the information in the instrument manual and
supplementary information (this can often be chemical in nature).
5. Where staff are not adequately qualified provide adequate
supervision to ensure that safety critical work is properly carried out;
6. Ensure that the calibrations performed, and any correction
factors adopted, are relevant, and adequate, for the task being performed; and
the end use of the data.
7. Ensure that the mission critical nature of the results,
and the potential for inaccuracies, have been recognised in your safety risk
assessments.
8. Contact the AGS Loss Prevention - Chemical Safety Hot Line
for further information, if required.
TC White Marquis & Lord
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A national archive of site
investigation data
As aired at the recent AGS Format discussion session
following the presentation by Jeremy Giles from BGS, the concept of a national
archive of site investigation data is unquestionably an excellent resource.
However, the users of this facility are frequently frustrated by the
'unavailability' of some of the archive due to confidentiality agreements that
require the BGS to not release such information to third parties. Searches by
BGS against a specific location requested by a user, provide neighbouring site
investigation information and print-outs of such references together with a
location map indicating their sites. The user can then request either a postal
or first hand study at Keyworth of a selection of such data. At this point BGS
may not be able to provide all data as some of it is reserved for their
exclusive use in improving the national understanding of this field of study.
Jeremy Giles agreed this was an issue but that BGS was
powerless to circumnavigate such agreements. On an occasion when it had been
found to have inadvertently issued such confidential data, the original sender
of information had recalled all its previously lodged records! In a converse
situation, a searcher of the records cited an occasion where, having found some
data 'blocked' by BGS, contacted the original depositing company who quickly
agreed to remove such exclusivity. The additional desk study information was
subsequently released to the searcher following a formal letter from the
depositor to BGS.
It was suggested that there should be some time bar
attributable to such confidentiality agreements so that after an agreed time,
the information was then allowed to be available to all. Thus AGS members may
like to consider the incorporation of a common clause into their contracts
stating that unless the Client expressly refused permission, the site
investigation information would be sent to BGS and, after a period of time,
become publicly available under normal BGS arrangements. The obvious debate to
be had before this could be forwarded as a suggestion to BGS, is to define an
agreed period of time.
The Client would presumably wish have a period of
confidentiality so as to secure their commercial objective in obtaining the
information. It is suggested that most AGS practitioners would not be too
concerned as to the time period, other than easing the real problem of
archiving! A period of six years may be appropriate, as much of the site
investigation work in the UK is effectively carried out under hand, rather than
sealed, contracts.
John Hislam
Applied Geotechnics
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Management
of Risk Associated with Ground Reports
Michael Joyce, a chartered engineer,
chartered geologist and chartered arbitrator, has written to the AGS in
connection with some of our observations about the effectiveness of arbitration in
the AGS document Management of Risk Associated with the Preparation of Ground
Reports - Guidelines for the Preparation of the Ground Report.
In brief terms, the authors of the
document (at paragraph 4.4.9) express a preference for litigation because of the
legal expertise of judges, their increasing technical understanding and, most
importantly, their willingness to deal swiftly and decisively with unsustainable
negligence allegations raised simply as a means of avoiding or delaying payment
to a specialist. Mr Joyce points out that most arbitrators nowadays have had
some legal training and have the benefit, over judges, of being qualified
technically in the subject area of the dispute. In his experience, arbitrators
will take a robust and harsh line with those presenting bogus negligence claims
as a way of circumventing a specialist's entitlement to his fee for the work
undertaken.
Mr Joyce's views demonstrate, at the very least, the dramatic
differences in the views of some lawyers
and engineers regarding the relative merits of arbitration and litigation. AGS
members should therefore be aware that although the authors of the AGS Guidelines
for the Preparation of the Ground Report generally prefer litigation to
arbitration, many experienced practitioners have the opposite opinion.
Steven Francis
Eversheds LLP Solicitors
Chairman
AGS Loss Prevention Working Group
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=======================================
Guidelines for the
Preparation of the Ground Report / Management of Risk Associated with Ground
Reports
These documents form the two parts of the latest AGS
publication and form an invaluable guide for everyone involved in the
preparation of Ground Reports.
Copies have been distributed to all Members and further ones
can be purchased for £12.50 (including p+p).
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BRE SD1:2005 - Implication for SI
& Specifications
The Building Research Establishment (BRE) has recently
revised Special Digest 1 "Concrete in aggressive ground". This new
edition (SD1: 2005), funded by The Concrete Centre, was published as a single
volume in June, following the completion of a four year research programme on
combating the thaumasite form of sulphate attack (TSA) . There are two key
changes to the procedure for assessing the ground;
1. The limits of the design sulphate classes based upon 2:1
water/soil extract tests on soil have been reduced to bring sulphate
classifications based on 2:1 water/soil extract tests and on groundwater into
parity. This will result in some sites being rated as more aggressive to
concrete than hitherto.
2. High magnesium levels are no longer taken into account for
natural ground.
There are five key changes to the procedure for the
specification of concrete;
1. The recommended maximum water/cement ratios and the
minimum cement contents have been revised.
2. A new classification for cements and blended cements has
been introduced to harmonise with European standards.
3. The recommended concrete quality now caters for the
inherent possibility of exposure to an external source of the carbonate required
for TSA.
4. The number of additional protective measures to be applied
at higher sulphate levels has been reduced, in general by two.
5. The use of the concept 'intended working life' replaces
that of 'structural performance level' to harmonise with European standards.
BRE has told FPS that the take up of its revised SD1 would
likely be slow as it has received no funding to mount a promotional campaign. It
is relevant to note that currently some of the on-line information services are
still offering just the SD1:2003 version, some 6 months after publication of the
latest edition. Also, even if professionals do know of the existence of
SD1:2005, they may not feel obliged to use it at the moment as the current
edition of BS 8500 Concrete refers to SD1:2003. BS 8500 will unlikely to be
updated before the latter part of 2006.
It is often not clear which version of SD1 has been
used to classify the ground and the concrete.
The members of the Federation of Piling Specialists (FPS) are
supplied with numerous site investigation reports and Engineer's Particular
Specifications every working day. Currently it is often not clear in these which
version of SD1 has been used to classify the ground and the concrete. It is the
exception when clear reference is made to say SD1: 2005.
FPS requests that in future all site investigation reports
and Particular Specifications make clear reference to SD1: 2005. Our Clients can
then be confident that piling concrete is provided in accordance with the latest
requirements by eliminating the potential for misunderstanding to enter into the
specification process.
Grout is a different material to concrete and
SD1:2005 is only applicable for concrete.
In addition, FPS also requests that where the foundation
solution may comprise minipiles, ground anchors, soil nails, grouting, base or
shaft grouted piles, permanent sleeves to piles, or cross-hole sonic logging of
piles, i.e. any case where grout is likely to be used either in lieu of, or in
addition to, concrete, that reference is not made to SD1: 2005 for these
options. This is due to the fact that grout is a different material to concrete
and SD1: 2005 is only applicable for concrete.
Tony Suckling
Technical Development Manager Stent Foundations Ltd
Chair Technical Committee
Federation of Piling Specialists
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CLAN 02/05
In September 2005, the Cabinet Office led Soil Guidance Value
(SGV) Task Force issued its first (and long awaited) public pronouncement -
Contaminated Land Advice Note No. 2 [CLAN 02/05]. This Note has far reaching
consequences and effectively signals a change of interpretation (if not policy)
at the Environment Agency/ DEFRA. [www.defra.gov.uk/environment/land/contaminated/pubs.htm].
The SGV Task Force was set up following a 'stakeholder
workshop' in November 2004, at which the AGS was well represented. Simon Edwards
(Merebrook) and Seamus Le Froy Brookes (LBH Wembley) have since attended Task
Force meetings on behalf of the AGS - and the views of the AGS were canvassed by
means of a 'Mirror Group' and via the normal meetings of the Contaminated Land
Working Group.
The remit of the Task Force is very wide, embracing matters
as diverse as the continuing professional development of those involved in
contaminated land through to the detail of toxicological risk assessment.
It has been recognised by industry for some time that some of
the published SGVs were at concentrations at or around background
concentrations. There must be very few working in this area who have not
struggled with the benzo(a)pyrene question! However, the initial view of the
Health Protection Agency (HPA) and Environment Agency regulators were that these
were very hazardous chemicals and exposure should therefore be kept as low as
possible. A year of persuasion has now borne fruit in the form of CLAN 02/05
which formally recognises that there is a big difference between the published
SGVs and the concentrations of contaminants in the soil which would be capable
of presenting a real hazard to people living on that land - in the terminology
"a significant possibility of significant harm" [or SPOSH - how we
love our acronyms!].
In some of the key sections, this Note, comments that:
-
SGVs mark the concentration of contamination in soil
where tolerable or minimal risks would result from exposure
-
Exceedence of the SGV indicates further assessment or
remedial action may be needed
-
Concentrations at or marginally above SGVs would not
necessarily meet the legal tests [in Circular 02/2000], for determining
"Contaminated Land" (as defined in Part IIA of the Environmental
Protection Act 1990).
Of course, helpful as these statements are, one key question
now begs to be answered. Namely, how far above the SGV does the concentration
have to be to meet the "unacceptable intake" test. In the deadpan
language of Sir Humphrey, CLAN 02/05 says that "at the present time the
published Defra/Environment Agency technical guidance on risk assessment does
not address this issue". Clearly, the publication of such guidance is
critical. No timetable has been set by the Task Force, but the clamour from both
regulator and regulated for urgent resolution, surely can not be ignored.
Of course one has to ask where this leaves all those affected
by sites designated by local authorities as "Contaminated Land" on the
basis of marginal exceedence of SGVs.
The work of the SGV Task Force continues, no longer under the
auspices of the Cabinet Office, but under English Partnerships' Brownfield
Strategy, under the chairmanship of Jane Forshaw (CEO of CL:AIRE (Contaminated
Land: Applications in Real Environments)). There is no doubt that pressure from
industry and political determination at the Cabinet Office has at last made real
progress but much remains to be done. In addition to the thorny issue of what
constitutes soil concentrations capable of providing an unacceptable intake,
progress on the publication of the SGVs themselves remains painfully slow.
The Agency has recently released the updated version of the
CLEA UK risk assessment model for a trial period until April 2006 [www.environment-agency.gov.uk].
Formal ratification and publication of that model remains high on industry's
agenda.
It is clearly vital that the momentum needed to make progress
in all these areas, which has started to develop as a result of the Task Force,
must continue. The AGS will of course continue to support its work but it is
vital that the absence of the Cabinet Office does not allow Defra/ the EA and
the HPA to return to the previous snail's pace.
Hugh Mallett
Enviros
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Copyright Regulations
Potential Loss Risk or a Hidden sources of Revenues
Every document issued in the pursuit of producing site
investigation information is in some way affected by:
Copyright and Related Rights Regulations 2003 SI No. 2498
Many people are unaware of the important changes in the law
brought about by the enactment of these regulations in October 2003. The key
point of note with respect to site investigation work is the changes in the law
regarding the copying of documents for research. This is a key factor in the
production of desk studies.
There is useful a document available for download from the
Copyright Licensing Agency (CLA) at:
http://www.cla.co.uk/support/business/guidance-for-businesses.pdf
It states in this document that:
"..under the old law, copying undertaken for research or for private
study was an exception; provided that the copying could be classed as 'fair
dealing'.."
It goes on to say that:
"Under the new law, any copying for research or private study, which is
carried out for a commercial purpose, will require prior permission from the
copyright owner or a CLA license to permit certain copying."
Conversely documents produced by business are now better
protected and rights to further payments for multiple reproductions of reports
are inherently supported more strongly by the change in the law.
There may be exceptions to the regulation where the documents
being produced incorporate copies of other works are expressly for the use of a
court of law or recognised arbitration body. However, individual circumstances
should be checked as there may be case specific exceptions.
The CLA operates a free help line to answer queries about
copyright and the need for licenses: 0800 085 6644
Loss Prevention Measures
1. Obtain a copyright license relevant to your business.
2. Where an item is not covered by the license obtain
permission to copy from the author, or rights owner.
3. Study CLA guidance in this area.
4. Protect your own copy right, where appropriate.
5. When producing documents consider what reasonable charge
you might make for its reproduction in advance of being asked.
6. If you chose to allow reproduction seek legal advice on
the reliance others may place on it as a result of you granting permission for
copying and distribution.
TC White
Marquis & Lord
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